Tuesday, August 04, 2009
Spinal Cord Injury Repair
We wanted to share a recent publication authored by Dr. Mark Tuszynski and his team of researchers at USCD. Here's the good news:
"NT-3 expression in the correct target led to reinnervation of the nucleus gracilis in a dose-related fashion, whereas NT-3 expression in the reticular formation led to mistargeting of regenerating axons. Axons regenerating into the nucleus gracilis formed axodendritic synapses containing rounded vesicles, reflective of pre-injury synaptic architecture. Thus, we report for the first time, to the best of our knowledge, the reinnervation of brainstem targets after SCI and an essential role for chemotropic axon guidance in target selection"
Laura Taylor Alto, Leif A Havton, James M Conner, Edmund R Hollis II, Armin Blesch & Mark H Tuszynski. Chemotropic guidance facilitates axonal regeneration and synapse formation after spinal cord injury. Nature Neuroscience. Published online: 2 August 2009 doi:10.1038/nn.2365.
Featured Neuromics Reagent
NT-3
Related Reagents:
Neurotrophins and Growth Factor Antibodies
Neuron/Glial Marker Antibodies
Neurotrophins-Neuron/Glial Marker Proteins
Stem Cell Reagents
Here's to finding the cure!
Thursday, July 30, 2009
FGF Basic and Cell Proliferation in Endothelial Cells
Here's a recent publications referencing use of our FGF basic in Endothelial Cell Cultures.
Harun Elmasri, Cagatay Karaaslan, Yaroslav Teper, Elisa Ghelfi, MeiQian Weng, Tan A. Ince, Harry Kozakewich, Joyce Bischoff, and Sule Cataltepe. Fatty acid binding protein 4 is a target of VEGF and a regulator of cell proliferation in endothelial cells. FASEB J, Jul 2009; doi:10.1096/fj.09-134882
...VEGF-A 165 (VEGF) and human basic FGF (bFGF) were purchased from R&D Systems (Minneapolis, MN, USA) and Neuromics (Edina, MN, USA), respectively...
Featured Reagent
FGF basic (146 aa)
Related Reagents:
Proteins
FGF basic (146 aa), carrier-free
FGF basic (157 aa)
FGF basic (157 aa), carrier-free
Fibroblast Growth Factors
Antibodies:
FGF2
All Stem Cell Reagents
Monday, July 27, 2009
TRPA1 in Craniofacial Muscle Pain
Jin Y. Ro, Jong-Seok Lee and Youping Zhang. Activation of TRPV1 and TRPA1 leads to muscle nociception and mechanical hyperalgesia. doi:10.1016/j.pain.2009.04.021.
... TRPA1 (1:1500; rat polyclonal, Neuromics)...
Featured Reagents
TRPA1-Cat#: RA14135
Related Reagents:
TRPA1 for WB
VR1 N-Terminus (TRPV1)
VR1 C-terminus (TRPV1)
VR1 C-Terminus (TRPV1) - mouse specific
VR1 (TRPV1)-Goat
VR like-3 (TRPV3)
All TRPV (Vanilloid); TRPM; TRPA and TRPCs
Pain and Inflammation Antibodies
Sunday, July 26, 2009
STEMEZ hN2 Human Neurons-Data
Applications for these include: cellular model studies, high content screening, developmental studies, RNAi studies and genetic manipulation.
Drilling down further, I am pleased to present Electro-physiology and related data generated by Aruna and collaborators: hN2 Cells-Electro Phys Data Supplement
hN2-Whole Cell Voltage ClampFigure. hN2 cells can produce inward currents that generate action potentials. (A) Isolated hN2 with significant neurite growth 1 week after plating . This cell was subjected to whole cell voltage clamp utilizing a potassium gluconate based intracellular solution. (B) Voltage gated inward and outward currents were elicited from this cell with depolarizing voltage steps. (C) Inward currents from another cell (potassium gluconate intracellular) were abolished by local application of 1 µM tetrodotoxin (red trace) while outward currents remained. Inward current recovered as TTX washed out of the region (green trace). (D) A different cell which exhibited voltage activated inward currents that inactivated in response to a 50 ms prepulse at different membrane potentials. The experiment was done 27 days after the removal of bFGF. A cesium gluconate based intracellular solution was used for this experiment to block outward potassium currents. The membrane potential for half maximal inactivation by standard Boltzman fitting (red line) was -40.1 mV with a slope of 4.7. (E) Recovery from fast inactivation utilizing a paired pulse protocol in the same cell as C. The single exponential time constant for recovery of inactivation was 1.7 ms (red line). (F) A different cell which elicited an overshooting action potential upon current injection under whole cell current clamp utilizing a potassium gluconate based intracellular solution. Inset: Response of the same cell under voltage clamp to a change in membrane potential from -80 mV to -10 mV elicited a peak current of 457 pA. Scale bars for inset: 5 ms, 0.2 nA.
Thursday, July 23, 2009
Stem Cell Markers
In this study the authors demonstrate a between SSCs and RET.
ETV5 is expressed beginning in fetal Sertoli cells and can potentially have effects on both neonatal Sertoli and germ cells. In addition, ETV5 has critical effects on neonatal spermatogonial proliferation, which may involve impaired signaling through the RET receptor.
Gaurav Tyagi, Kay Carnes, Carla Morrow, Natalia V. Kostereva, Gail C. Ekman, Daryl D. Meling,
Chris Hostetler, Michael Griswold, Kenneth M. Murphy, Rex A. Hess, Marie-Claude Hofmann and Paul S. Cooke. Loss of Etv5 Decreases Proliferation and RET Levels in neonatal Mouse Testicular Germ Cells and Causes an Abnormal First Wave of Spermatogenesis. DOI:10.1095/biolreprod.108.075200
Images: Ret IHC in WT and Etv5-/- testes (n=4). The intensity of RET staining per spermatogonia is markedly reduced in Etv5-/- testis (B) even though the number of cells staining for RET are comparable to the WT (A) testis. Insets are higher magnification of spermatogonia showing differences in staining intensity. Bars = 50 μm in A and B, insets = 10 μm.Patent:Neuronal progenitors from feeder-free human embryonic stem cell culture.
Inventor: Stice, et al.
Date Issued: May 12, 2009
Application: 11/243,819
Inventors:
Stice; Steve (Athens, GA)Shin; Soojung (Baltimore, MD)Dhara; Sujoy (Athens, GA)
Assignee:
University of Georgia Research Foundation, Inc. (Athens, GA)Include use of Nestin antibody
Stem Cell Antibodies
Stem Cell Research Proteins
Neural Stem Cells and Media
Neuroprogenitor Neurosphere Tissue-NEW!
Neuroprogenitor Neurosphere tissue is provided live, unseparated, fresh from E18 rat cortex/hippocampus including subventricular zone.
Expansion/Differentiation Kits
FACS/Phenotyping
Related Reagents:
Neurotrophin and Growth Factor Antibodies
Neurotrophin Proteins
Tuesday, July 21, 2009
Sunday, July 19, 2009
Friday, June 26, 2009
Hes-1 and Develpmental Neurobiology
Angelo Iulianella, Madhulika Sharma, Greg B. Vanden Heuvel, and Paul A. Trainor. Cux2 functions downstream of Notch signaling to regulate dorsal interneuron formation in the spinal cord. Development 136, 2329-2334 (2009). doi: 10.1242/10.1242/dev.032128.
...anti-Hes1 (Neuromics, Edina, MN, USA)...
Related Reagents:
Sunday, June 14, 2009
Potent Stem Cell Markers
Here're the latest:
Saishu Yoshida, Takako Kato, Takao Susa, Li-yi Cai, Michie Nakayama, Yukio Kato. PROP1 coexists with SOX2 and induces PIT1-commitment cells. Biochemical and Biophysical Research Communications, Volume 385, Issue 1, 17 July 2009, Pages 11-15
... SOX2 (1:500 dilution, Neuromics, Edina, MN, USA)...
Saravanan Karumbayaram, Bennett G. Novitchb, Michaela Patterson, Joy A. Umbach, Laura Richter, Anne Lindgren, Anne E. Conway, Amander T. Clark, Steve A. Goldman, Kathrin Plath, Martina Wiedau-pazos, Harley I. Kornblum, William E. Lowry. Directed Differentiation of Human-Induced Pluripotent Stem Cells Generates Active Motor Neurons. Stem Cells Vol. 27 No. 4 April 2009, pp. 806 -811. doi:10.1002.
... mouse anti-Nestin (Neuromics)...
Patrizia Rubini, Javorina Milosevic, Johannes Engelhardt, Mahmoud Al-Khrasani, Heike Franke, Attilla Heinrich, Beata Sperlagh, Sigrid C. Schwarz, Johannes Schwarz, Wolfgang Nörenberg and Peter Illes. Increase of intracellular Ca2+ by adenine and uracil nucleotides in human midbrain-derived neuronal progenitor cells. Cell Calcium. Volume 45, Issue 5, May 2009, Pages 485-498.
...rabbit anti-P2Y2 (1:1000; Neuromics, Edina, MN, USA...
Thursday, May 07, 2009
Detecting Apoptosis in Real Time
Aaron J. Thomas and Carol A. Erickson. FOXD3 regulates the lineage switch between neural crest-derived glial cells and pigment cells by repressing MITF through a non-canonical mechanism. Development, Apr 2009; doi:10.1242/dev.031989.
...Apoptosis was assayed using Magic Red Caspases 3&7 reagent (Neuromics)...
Related Reagents:
FLIVO™ Polycaspase Live!, in vivo Apoptosis Kits-New
FLICA™ in vitro Caspase Kits
Fast!-Use Caspase kits to quantitate apoptosis via active caspases in whole, living cells. These kits do not use ELISA or any antibodies for detection
FLISP™ Serine Protease Detection Kits
Measure chymotrypsin-like proteaseactivation in whole living cells.
MitoPT™ Kits
Quantitate mitochondrial functionality and apoptosis
Apoptosis Research Antibodies
Apoptosis Research Proteins
Thursday, April 02, 2009
RAGE and Pneumonia
An interesting finding on Receptor for Advanced Glycation End Products (RAGE) and response to S. pneumoniae pneumonia infection just crossed our radar. Dr. Marieke A. D. van Zoelen and team published evidence that RAGE plays a detrimental role in the host response to S. pneumoniae pneumonia by facilitating the bacterial growth and dissemination and concurrently enhancing the pulmonary inflammatory and procoagulant response. Data include use of our RAGE-Cat#: GT15030.
Here's the publication and related data:
Marieke A. D. van Zoelen, Marcel Schouten, Alex F. de Vos, Sandrine Florquin, Joost C. M. Meijers, Peter P. Nawroth, Angelika Bierhaus, and Tom van der Poll. The Receptor for Advanced Glycation End Products Impairs Host Defense in Pneumococcal Pneumonia. J. Immunol., Apr 2009; 182: 4349 - 4356.
...Endogenous peroxidase activity was quenched using 1.5% H2O2 in PBS. Primary Abs used were goat anti-mouse RAGE polyclonal Abs (Neuromics), and secondary Abs were biotinylated rabbit anti-goat Abs (DakoCytomation). ABC solution (DakoCytomation) was used as the...
Images: Expression of RAGE in lungs during S. pneumoniae pneumonia. Representative view of a lung from a normal, uninfected Wt mouse (A) displaying ubiquitous expression of RAGE on the surface of endothelium. B, Absence of RAGE positivity in the lung of a RAGE–/– mouse. C and D, Lungs from a Wt mouse 48 h after the inoculation of S. pneumoniae. Arrow indicates bronchial epithelium in healthy lungs (A); asterisk indicates neutrophils in an area with confluent pneumonia (D), both being negative for RAGE staining. RAGE staining: original magnification x10.Realted Reagents:
RAGE Mouse Mononclonal
Immune Response Antibodies
Immune Response Proteins
Monday, March 30, 2009
Introducing Human Neuron Kits
hN2 Human Neurons Discovery Kit-NewEnergize you Research!
Neuromics has formed an alliance with Aruna Biomedical. This Alliance gives us the capabilities to bring you the reliable, robust and highly scalable hN2TMHuman Neurons Discovery Kits.
These kits are designed to reduce basic Neuroscience Research and Drug Discovery timelines. Potential applications include: cellular model studies, high content screening, developmental studies, RNAi studies and genetic manipulation.
Approximate Yield=1,000,000 healthy Neurons.
hN2 Human Neurons Discovery Kit Details
Friday, March 13, 2009
Amyloid Beta and E18 Primary Hippocampal Neurons
Related Publication:
Karunya K. Kandimalla1, Olenych G. Scott, Smita Fulzele1, Michael W. Davidson, Joseph F. Poduslo. Mechanism of Neuronal versus Endothelial Cell Uptake of Alzheimer's Disease Amyloid β Protein. PLoS ONE 4(2): e4627. doi:10.1371/journal.pone.0004627.
... Rat primary hippocampal (RPH) neurons were isolated from the hippocampii of 18-day-old embryonic Sprague Dawley rat brains (Neuromics, Edina, MN). The hippocampii were dispersed using a fire polished Pasteur pipette and plated on poly-D-lysine (Sigma-Aldrich, St. Louis, MO) coated glass cover slips in B-27 neurobasal medium containing 0.5 mM glutamine and 25 µM glutamate (Invitrogen, Carlsbad, CA). The neuronal cells were grown under 5% CO2 in an incubator maintained at 37°C until differentiation...
Images: A–D: Uptake of fluorescein labeled Aβ40 (F-Aβ40) and Alexa Fluor® 633 labeled transferrin (AF633-Trf), clathrin-mediated endocytosis marker, in rat primary hippocampal (RPH) neurons following 30 min incubation at 37°C. (A) F-Aβ40 uptake; (B) Uptake of AF633-Trf; (C) Superimposition of images A and B; (D) Overlay of fluorescence images on the DIC image of RPH neurons. E–G: Uptake of F-Aβ40 and AF633-Trf in RPH neurons at 4°C. (E) Uptake of F-Aβ40; (F) No significant neuronal uptake of AF633-Trf at 4°C; (G) Superimposition of images D and E on the DIC image of RPH neurons; H–J: Uptake of F-Aβ40 and AF633-Trf in RPH neurons treated with 10 mM Sodium Azide and 50 mM 2-deoxy glucose, agents that are known to deplete cellular ATP. (H) Uptake of F-Aβ40; (I) No significant cellular uptake of AF633-Trf was observed; (J) Superimposition of images H and I on the DIC image of neurons.doi:10.1371/journal.pone.0004627.g010
Saturday, February 28, 2009
TRPV1 with a Twist
Ann M. Bode, Yong-Yeon Cho, Duo Zheng, Feng Zhu, Marna E. Ericson, Wei-Ya Ma, Ke Yao, and Zigang Dong. Transient Receptor Potential Type Vanilloid 1 Suppresses Skin Carcinogenesis.Cancer Res., Feb 2009; 69: 905 - 913.
"TRPV1 interacts with EGFR, leading to EGFR degradation. Notably, the absence of TRPV1 in mice results in a striking increase in skin carcinogenesis. The TRPV1 is the first membrane receptor shown to have a tumor-suppressing effect associated with the down-regulation of another membrane receptor."
...dorsal skin samples (100 mum) were processed and immunostained. For the human skin cancer tissue array, we used anti- TRPV1 -(Neuromics), anti-EGFR (Cell Signaling), and Alexa Fluor 488 and 647-conjugated secondary antibodies. Mouse skin samples were immunostained...
Sunday, February 22, 2009
TRPV1 and Retinal Ganglion Cell Apoptosis
...we used rabbit anti-mouse TRPV1 IgG (1:500; catalog number RA14113; Neuromics, Edina, MN) against the absolute C terminus of mouse TRPV1 (EDAEVFKDSMAPGEK)...
TRPV1 localization in RGCs of rat retina. (A) Immunocytochemical labeling for TRPV1 shows strong localization in the outer retina and in RGCs (large cell bodies); there is little or no label in smaller displaced amacrine cells of the GCL. Clear examples of amoeboid-shaped cell bodies of microglia cells are indicated (ovals). Right: Control section preabsorbed using the TRPV1 blocking peptide (+BP). (B) Confocal image stack through GCL and NFL showing labeling for TRPV1 in wholemount preparation counterlabeled with antibodies against heavy-chain neurofilaments that recognize broad-field RGCs (SMI32). Image shows punctate localization to dendrites (arrows) as well as intense label to cell bodies (brackets); smaller cell bodies with TRPV1 label are in the background. (C) Confocal image stack through GCL and NFL of peripheral retina shows TRPV1 in RGC cell bodies (bracket) and in small bundles of RGC axons (arrows). (D) Confocal stack from central retina shows TRPV1 in RGC cell bodies (bracket) and in axon bundles in the NFL as they course toward the optic nerve head. Amoeboid-shaped cell bodies of microglia are apparent (ovals). (E) Confocal image in single plane at GCL/NFL border shows Iba-1–labeled microglia processes colocalizing with TRPV1, as we previously demonstrated.51 TRPV1-label RGC cell bodies (brackets) and axons (arrows) are indicated for reference. (F) Immunocytochemical labeling demonstrates strong perinuclear and dendritic localization of TRPV1 in cultured RGCs counterstained with the nuclear label DAPI. Localization to dendritic processes and neurites (dashed circles) includes node-like clusters; right: these regions are shown at higher magnification. (G, top) Western blot against TRPV1 in brain and whole retina from adult rat shows band at expected molecular weight (arrowheads; 100–113 kDa). Retina demonstrates an additional band with a slightly lower molecular weight that probably corresponds to a different glycosylation state for this antibody.79 Bottom: Control Western blot with preabsorption of TRPV1 antibody using the blocking peptide prevents detection of both bands. ONL, outer nuclear layer; OPL, outer plexiform layer; INL, inner nuclear layer; IPL, inner plexiform layer; GCL, ganglion cell layer; NFL, nerve fiber layer.Thursday, February 19, 2009
Neurotrophin Expression in Airway Smooth Muscle Cells
Y.S. Prakash, Michael A Thompson, and Christina M Pabelick. Brain Derived Neurotrophic Factor in TNF Modulation of Ca2+ in Human Airway Smooth Muscle. Am. J. Respir. Cell Mol. Biol., Feb 2009; doi:10.1165/rcmb.2008-0151OC.
... goat polyclonal anti-TrkB-Cat#: GT15080 (Neuromics, Minneapolis, MN; 1:1000 dilution)...
Featured Reagents
TrkB-Cat#: GT15080
TrkB-Cat#: MO15042
Related Reagents:
TrkB-Cat#: MO15025
TrkA for FC
TrkA-Cat#:MO15018
TrkA Cat#: MO15034
TrkA Cat#: GT15153
TrkC-Cat#:MO15000
All Neurotrophins and Growth Factor Antibodies
All Neurotrophins-Neuron/Glial Marker Antibodies
Thursday, February 12, 2009
Substance-P Pub
Coexpression of 2A-adrenergic and -opioid receptors in substance P-containing terminals in rat dorsal horn. The Journal of Comparative Neurology Volume 513 Issue 4, Pages 385 - 398 Published Online: 29 Jan 2009 Copyright © 2009 Wiley-Liss, Inc., A Wiley Company.
...guinea pig anti-SP (1:500; Neuromics Antibodies)...

Substance P-Rabbit
Substance P-Mouse
Neurokinin-1 (NK 1) (RA25001)
Neurokinin-1 (NK 1) Human (RA25003)
Neurokinin-3 (NK 3) (RA25001)
proNeurokinin B (proNKB or P2)
All Neuropeptides
Image: Immuofluorescent detection of Substance P in rat spinal cord dorsal horn (red fluorescence). DAPI (blue) was used as counter stain.
Friday, January 23, 2009
Opioid Receptor Antibodies that Rock
They are extensively referenced. We feature select publications and are pleased to feature the latest referencing staining of mouse neurons using our Kappa Opioid Receptor.
...Dominika Labuz, Yvonne Schmidt, Anja Schreiter, Heike L. Rittner, Shaaban A. Mousa and Halina Machelska. Immune cell–derived opioids protect against neuropathic pain in mice. J. Clin. Invest. doi:10.1172/JCI36246. Copyright © 2009, The American Society for Clinical Investigation...
...κ-opioid receptor (1:800, Neuromics)...
All Opioid Receptor Publications-Mu, Kappa and Delta
Published Reagents:
Mu Opioid Receptor-Rabbit
Mu Opioid Receptor-Guinea Pig
Delta Opioid Receptor 358-372
Kappa Opioid Receptor
Related Reagents:
Opioid Receptors
All Pain and Inflammation
Wednesday, January 14, 2009
24-OHC-27-OHC and Alzheimer's
27-OHC increased levels of amyloid precursor protein (APP) as well as beta-secretase (BACE1)
the enzyme that cleaves APP to yield Abeta, a molecule that causes alzheimer's.
24-OHC are associated with increased levels of sAPPalpha, suggesting that 24-OHC favors the processing of APP to the non-amyloidogenic pathway.
Futher study of this relationship between 27 and 24-OHC could yield possible targets for decreasing the cleavage of alzheimer's causing proteins and result in more step towards the Azheimer's therapies.
Here's the publication.
Prasanthi JRP, Huls A, Thomasson S, Thompson A, Schommer E, Ghribi O. Differential effects of 24-hydroxycholesterol and 27-hydroxycholesterol on beta-amyloid precursor protein levels and processing in human neuroblastoma SH-SY5Y cells. Molecular Neurodegeneration 2009, 4:1 (6 January 2009).
Image:

Treatment with 24-OHC, but not with 27-OHC, increased ABCA1 and ABCG1 levels. Representative Western blots
Monday, January 12, 2009
December 2008 Featured Pubs
Another publication referencing successful delivery of siRNA using i-Fect
Suneeta Tumati, Tally Largent Milnes, Henry I. Yamamura, Todd W. Vanderah, William R. Roeske and Eva V. Varga. Intrathecal Raf-1-selective siRNA attenuates sustained morphine-mediated thermal hyperalgesia. doi:10.1016/j.ejphar.2008.10.033
...siRNAs stock solutions (100 ?M) were prepared in double distilled RNAse free water and stored in aliquots at ?80 °C. For intrathecal treatment, aliquots of the stock solution (2 ?g of the appropriate siRNA) were mixed (1:5 v/v)with i-Fect transfection reagent (Neuromics, Edina, MN). After recovery from the surgery (5-7 days), the animals received intrathecal injections (2 ug! siRNA/1 0 ul/rat) of either a lipid encapsulated Raf-1-selective siRNA mixture (Smart pool siRNA, Dharmacon Inc; Chicago, IL, Cat # L-087699-00) (Raf-1 siRNA groups) or i-Fect encapsulated non-targeting dsRNA (Dharmacon, #D-001810-01-20) (control mismatch siRNA groups) or the transfection lipid alone, once daily, for 3 days, as described earlier (Gardell et al., 2002). Intrathecal injections of the siRNAs or the transfection agent alone did not cause any sign of behavioral toxicity. Western blots, using a Raf-1-selective antibody, indicated that intrathecal treatment with the Raf-1-selective siRNA mixture for 3 days significantly reduced Raf-1 protein levels in the dorsal root ganglion and in the dorsal horn of the spinal cord..
Lasani S. Wijetunge, Sally M. Till, Thomas H. Gillingwater, Cali A. Ingham, and Peter C. Kind. mGluR5 Regulates Glutamate-Dependent Development of the Mouse Somatosensory Cortex. The Journal of Neuroscience, December 3, 2008, 28(49):13028-13037; doi:10.1523/JNEUROSCI.2600-08.2008.
...Western blotting was performed as mentioned above and membranes were probed with antibodies against mGluR5 (1:4000, Neuromics)...
Saturday, November 22, 2008
Excellent TRPV1-N IHC and WB
detected by diaminobenzidine staining (DAB, Sigma, St. Louis, MO, USA). Sections were counterstained with hematoxylin, dehydrated, mounted with Pertex and studied. Goat serum was applied on control sections. Wednesday, November 12, 2008
DRG Neurons Now Available.
Primary Rat DRGs are live neurons isolated from micro-surgically dissected regions of day 18 embryonic Sprague/Dawley rat brain. These cells are prepared fresh each week and shipped in a nutrient rich medium that keeps the cells alive for up to 14 days under refrigeration.Please note: It is important to review Protocol/Datasheet prior to ordering. There is a unique step for making the dissociation enzyme solution. Do not hesitate to call or e-mail me (612-801-1007 or pshuster@neuromics.com) should you have questions.
-A dissection and Tissue Culture Manual of the Nervous System (1989). A. Shahar, J.D. Vellis, A. Vernadakis, B. Haber (Eds.), Dissociated Spinal Cord - Dorsal Root Ganglion Cultures on Plastic Tissue Culture Dishes and Glass Coverslips and Wells (pp.219-222). Wiley-Liss, Inc. J.L. Werth, -S.A. Thayer (1994) Mitrochondria Buffer Physiological Calcium Loads in Cultured Rat Dorsal Root Ganglion Neurons, The Journal of Neuroscience, 14(1), 348-356
Monday, November 03, 2008
Power Trio of Pain Research Antibodies
Shao-Rui Chen, Hao-Min Pan, Timothy E. Richardson, and Hui-Lin Pan. Potentiation of Spinal α2-Adrenoceptor Analgesia in Rats Deficient in TRPV1- Expressing Afferent Neurons. Published online 2007 March 24. doi: 10.1016/j.neuropharm.2007.03.009.

Images: Double immunofluorescence labeling showing α2C-AR- and TRPV1-immmunoreactivity in the spinal cord dorsal horn of one vehicle-treated and one RTX-treated rat. Representative confocal images showing α2C-AR- and VR1 C-terminus (TRPV1)-immunoreactivities in the spinal dorsal horn of one vehicle- and one RTX-treated rat. All images are single confocal optical sections. Scale bar, 100 μm. Inset: high-magnification images (scale bar = 10 μm) showing the distribution of α2C-AR- and TRPV1-immunoreactivity in the lamina I and II. Neuropharmacology. 2007 June; 52(8): 1624–1630.
Rabbit VR1 N-Terminus (TRPV1) is also referenced.
Related Reagents:
Alpha 2c
Pain and Inflammation Antibodies
Vision and Retina Antibodies
Thursday, October 16, 2008
Purinergic Receptor Pubs
In the first study 5 of our antibodies are used. It investigates the expression of purinergic P2 receptors in oxygen-induced retinal neovascularization.
Sylvia Sarman; Jorge Mancini; Ingeborg van der Ploeg; J. Oscar Croxatto; Anders Kvanta; Juan E. Gallo. Involvement of Purinergic P2 Receptors in Experimental Retinal Neovascularization. Current Eye Research. 10.1080/02713680701885470 .
...Five eyes (5 animals) from either hyperoxa- or non-hyperoxia-treated mice were enucleated and fixed for 48 hr at 4°C in paraformaldehyde (Sigma-Aldrich, St Louis, MO, USA). Afterward, eyes were immersed for cryoprotection in graded sucrose solution (5% overnight, 10%, 15%, and 20%) and interlocked with resin. Fourteen micron sections were obtained (Shandon AS325 Retraction Microtome, Thermo Scientific, Waltman, MA, USA) and fixed on polylysine-treated glass slides. After overnight incubation in primary antibody (P2X1 1:1000, P2X2 1:1000,P2X3 1:1000, and P2Y2 1:800) (Neuromics, Minneapolis, MN, USA) at 4°C, sections were treated with biotinylated secondary antibodies followed by an avidin peroxidase complex step (Vectastin Elite ABC, Vector Laboratories, Burlingame, CA, USA). Finally, a color reaction was obtained using 3,3'-diaminobenzidine (DAB)/nickel-enhanced solution for staining (Sigma-Aldrich, St Louis, MO, USA). At least 6 sections per retina were analyzed. For immunofluorescence, the sections were labeled with lissamine rhodamine-conjugated goat anti-rabbit Ig-G or with fluorescein-5-isothiocyanate-conjugated goat anti-guinea pig Ig-G (Jackson Immunoresearch Laboratories, West Grove, PA, USA). At least 6 sections per retina were analyzed. Visualization was done using a Nikon Fluorescence Eclipse Microscope (Tokyo, Japan), and photographs were taken with a Nikon DN 100 Digital Camera (Tokyo, Japan)...
Images: Expression of P2X and P2Y receptors in normal mice and in a model of ischemia-
induced pathological retinal angiogenesis as assessed by immunohistochemistry. (A) P2X2 receptor expression was found in the outer plexiform layer of control mice. (B) In micetreated with oxygen, the expression was similarly found in the outer plexiform layer. In addition, a strong signal was also found in the inner plexiform layer. This induction was noted in all slides analyzed. (C) Retina without primary antibody for P2X2. (D) In control mice,
weak P2Y2 receptor expression was seen in the ganglion cell and in the nerve fiber layer. (E) In mice treated with oxygen, P2Y2 expression
showed a similar overall distribution as control mice. The signal was, however, strongly up-regulated. This increase was noted in all slides analyzed. (F) Retina without primary antibody for P2Y2. Black bar = 20 μm.
The second studies P2Xs' role in neurotransmision.
Elsa Fabbretti*, Elena Sokolova*, Lara Masten, Marianna D’Arco, Alessandra Fabbro, Andrea Nistri and Rashid Giniatullin. Identification of negative residues in the P2X3 ATP receptor ectodomain as structural determinants for desensitization and the Ca2+ sensing modulatory sites. JBC Papers in Press. Published on October 8, 2004 as Manuscript M409772200.
...Western immunoblots of transfected or untransfected HEK cells were performed as recently reported (19). In brief, these were lysed using a buffer containing 100 mM Tris HCl (pH 6.8), 200 mM dithiothreitol, 4 % SDS, 20 % glycerol and a cocktail of protease inhibitors (Sigma), and separated on 10 % polyacrylamide gel. After blocking with Tris saline buffer (TBS) containing milk, Tween 20 and preimmune serum, proteins were incubated overnight at 4°C with an anti-P2X3 antibody (Neuromics; 1:2000). Immunocomplexes were incubated for 1 h with a peroxidase-conjugated secondary antibody (Sigma; 1:4000) and detected with a chemiluminescence ECL kit (Amersham). Negative controls were obtained by mock transfection of HEK cells with the pEGFP-N1 plasmid (CLONTECH). Controls for efficient loading of different lysate materials were carried out by using an anti-β actin antibody (mouse monoclonal, 1:2000, Sigma)...
Related Reagents:
P2X1-Rabbit Antibody
P2X2-Guinea Pig Antibody
P2X2-Rabbit Antibody
P2X3-Rabbit Antibody
P2X3-Guinea Pig Antibody
Related Reagents:
All Purinergic Receptor Antibodies
All Pain and Inflammation Antibodies
Vision and Retina Research Antibodies
Thursday, October 09, 2008
Neuron/Neuron Glial Markers
These reagents must work everytime in our customers' applications. Quality is confirmed by pro-active customers follow up and publication referencing the reagents.
Here we have several recent publications.
We are pleased to first feature Dr. Dr. Juana Maria Pasquini, University of and colleagues from University of Buenos Aires. She and her team use our Olig1,2,3 as a marker to study de-myelinating disease.
P.G. Franco, L. Silvestroff, E.F. Soto and J.M. Pasquini. Thyroid hormones promote differentiation of oligodendrocyte progenitor cells and improve remyelination after cuprizone-induced demyelination. doi:10.1016/j.expneurol.2008.04.039
...Olig 1-2-3 antibodies were from Neuromics Antibodies (Edina, MN); ...
Featured Product:
Related Products:
Antibodies:
Olig2
Neuron-Glial Markers
Neurotrophins and Growth Factors
Neurodegenerative Disease
Proteins:
Neurotrophins-Neuron/Glial Markers
Neurodegenerative Disease
SC Reagents
The second references one of our GFAP antibodies.
Sun Jin-qiao, Sha Bin, Zhou Wen-hao and Yang Yi. Basic fibroblast growth factor stimulates the proliferation and differentiation of neural stem cells in neonatal rats after ischemic brain injury. doi:10.1016/j.braindev.2008.06.005.
For the immunofluorescence assays, sections from the SVZ were washed (0.1 M Tris, pH 7.6, 15 min), denatured (2 N HCl, 37oC, 30 min), rinsed (0.1 M P10 min), incubated with 1% H2O2 in 0.1 M Tris for 30 min, rinsed, blocked (10% normal goat serum, 37oC, 30 min).
...GFAP (1:100, Neuromics)...
Saturday, October 04, 2008
siRNA-mediated gene silencing
She and her team have documented these in the publication:
For researchers desiring to effectively deliver siRNA to the CNS for gene expression of analysis of specific receptors, this publication offers proven methods. These include:
- The Choice of siRNA
- Choosing and Optimizing Transfection Reagents for siRNA Delivery to the Nervous System
- Delivery Systems-Microinjection and Infusion (using mini-osmotic pumps)
- Validation
We will continue to track advances by Dr. Lai and team
Wednesday, October 01, 2008
Skeletal Muscle Derived Stem Cell Markers
Tetsuro Tamaki, Yoshinori Okada, Yoshiyasu Uchiyama, Kayoko Tono, Maki Masuda, Masahiro Nitta, Akio Hoshi, Akira Akatsuka. Skeletal Muscle–Derived CD34+/45- and CD34-/45- Stem Cells Are Situated Hierarchically Upstream of Pax7+. Cells. Stem Cells and Development. August 1, 2008, 17(4): 653-668. doi:10.1089/scd.2008.0070....anti-nucleostemin (1:200; overnight; Neuromics, Edina, USA) for proliferative capacity...
Tuesday, September 23, 2008
Human Embryonic Stem Cell Differentiation Protocol
Elizabeth S Ng, Richard Davis, Edouard G Stanley & Andrew G Elefanty. A protocol describing the use of a recombinant protein-based, animal product-free medium (APEL) for human embryonic stem cell differentiation as spin embryoid bodies. Nature Protocols 3, - 768 - 776 (2008).
Friday, September 19, 2008
PDGFs in Non-small Cell Lung Cancer Tumor and Stromal Cells
I personally follow up with every customer that purchases our Cancer Research Reagents. This ensures they work as expected. In most cases, this is validate. If not, we fix the expressed issues.
We are now seeing more confirmation by the reagents being referenced in publications. In this publication, our PDGF-C antibody was used as a marker for Non-small Cell Lung Cancer Tumors.
"In univariate analyses, high tumor cell expression of PDGF-B (p 0.001), PDGF-C (p 0.01), and PDGFR- (p 0.026) were negative prognostic indicators for disease-specific survival."
Donnem, Tom MD, Al-Saad, Samer MD, Al-Shibli, Khalid MD, Andersen, Sigve MD, Busund, Lill-Tove MD, PhD, Bremnes, Roy M. MD, PhD. Prognostic Impact of Platelet-Derived Growth Factors in Non-small Cell Lung Cancer Tumor and Stromal Cells. Journal of Thoracic Oncology. 3(9):963-970, September 2008.
Featured Reagent:
PDGF-C
Related Reagents to Consider:
PDGF R Alpha
PDGF R Beta
VEGF/Flt-1
EGF
Cancer Antibodies
All Neurotrophin and Growth Factor Antibodies
Platelet Derived Growth Factor Proteins
Cancer Research Proteins
Neurotrophin and Growth Factor Proteins
Thursday, September 18, 2008
Rat Sensory Neurons and NK-1
Matt and his team at University of British Columbia study primary sensory nerve cells (neurons), which are responsible for the transmission of somatic (bodily) sensations such as touch, pain, hot, cold and so on from the periphery (skin, muscles and viscera) to the central nervous system (CNS, spinal cord and brain). His research extends to therapeutic potential of neurotrophins on regeneration in spinal cord injury and deafferentation pain.
In the past several years, he has generouly shared NT-3 and BDNF IHC data with us.
Here's a link to the publication:
Matt Ramer. Anatomical and functional characterization of neuropil in the gracile fasciculus. The Journal of Comparative Neurology. 10.1002/cne.21785.
Featured Reagent
Neurokinin-1 (NK 1) Receptor
Other Reagents to Consider:
Neurokinin-1 (NK 1) Human (RA25003)
Neurokinin-3 (NK 3) (RA25002)
Substance P (GP14103)
proNeurokinin B (RA25008)
All Neuropeptides
All Pain and Inflammation
Saturday, September 13, 2008
ELISA techniques and protocols
This teaching guide covers the three major types of ELISA: indirect, competitive, and sandwich. It integrates theory with practice, to help you understand what you are doing, and help you to do it!
Courtesy of our friends at Novus Biologicals.
Thursday, September 11, 2008
Ischemia, Inflammatory Response and Umbilical Stem Cells
Aaron Hirko, Renee Dallasen, Sachiko Jomura, Yan Xu. Modulation of Inflammatory Responses after Global Ischemia by Transplanted Umbilical-Cord Matrix Stem Cells. Stem Cells First published online August 21, 2008; doi:doi:10.1634/stemcells.2008-0075
Secondary to Cardiac Arrest is Brain Damage do to lack of blood flow. This is marked by a delayed loss of Neurons in CA1 hippocampus region of the brain due to inflammatory response.
The story timeline of this response is good then bad with interesting twists. The delay in neuronal loss is linked to initial inflammation. It involves both reactive astrocytes (astrocytosis) and glia. Delaying the loss is, of course, good.
...But then, the reactive astrocytosis and related glial scarring cause a physical and biochemical barrier to regeneration of neurons...a bad thing. Protecting the microglia is a good thing, because they these cells serve as scavengers for clearing the cellular debris. They can also secrete a variety of cytotoxic and protective chemicals.
The wow factor in this research is that implanted rat umbilical-cord matrix (RUCM) cells can provide partial protection against neuronal injury in rat brains. Rats treated with RUCM cells three days prior to an 8-min CA had only 25-32% neuronal loss in the hippocampal CA1 region compared to the typical 50-68% neuronal loss observed in the untreated or the vehicle-treated animals. This could be due to to the favaorable modulation of the "good-bad" inflammatory response.
The good news in the search for therapies for stroke and cardiac arrest victims is combined, stem-cell-like RUCM cells offer protection against neuronal injury after global cerebral ischemia by enhancing the survivability of the astroglia in the selectively vulnerable regions.
We are pleased that the research team used our GFAP antibody as an marker for astrotytic in their studies.
Monday, September 08, 2008
Neurotoxicity Testing
E18 and E20 Rat Primary Neuronal Tissue -NEURON CULTURES
E18 Rat Primary Neuronal Tissue - ASTROCYTE CULTURES
E18 Mouse Neuronal Tissue -NEURON CULTURES
E18 Mouse Neuronal Tissue -ASTROCYTE CULTURES
AND Apoptosis Research Re
agentsto help researchers more effectively study Neurotoxicity.
Images: Polycaspase Assay Kit, green was used to assess cell death in primay rat hippocampal neurons.Cells were plated on 25-mm poly-l-lysine-coated coverslips at 300,000 cells per coverslip. Cells were used at 4 or 8 days in vitro. Composite imagae (A) 3 out of 4 cells are apoptotic (green). No cells were necrotic as both of the PI-positive cells were FLICA-positive; they had compromised membranes and were probably in the late stages of apoptosis rather than necrosis. (B) 3 Caspase-positive cells fluoresce green.
Thursday, August 28, 2008
No Pain; No Gain

Monday, August 18, 2008
Transthyretin, αAPP peptides and Alzheimer's Disease
PLoS ONE. 2008; 3(8): e2899. Published online 2008 August 6. doi: 10.1371/journal.pone.0002899.
A-Beta proteolysis by TTR is KPI-sensitive.A- A-Beta incubated with TTR (A-Beta+TTR) shows a weaker A-Beta monomer band as compared to A-Beta alone (A-Beta), indicative of proteolysis, as analyzed by SDS-PAGE electrophoresis followed by western blot. Pre-incubation of TTR with pefabloc (A-Beta+(TTR+pefabloc)) and with an αAPP peptide containing the KPI domain (A-Beta+(TTR+KPI+−APP)) inhibits TTR proteolytic activity, whereas the αAPP peptide without the KPI domain (A-Beta+(TTR+KPI−−APP)) facilitates proteolysis. B- % of inhibition of TTR proteolysis by quantification of band intensity in A. C- Ultrastructural analysis by TEM of preparations incubated for 15 hours, as described in Materials and Methods. TTR inhibited A-Beta aggregation as compared with A-Beta incubated alone (upper panels). Pre-incubation of TTR with αAPP peptide containing the KPI domain (A-Beta+(TTR+KPI+−APP)) abrogated TTR ability to avoid A-Beta aggregation, whereas αAPP lacking the KPI domain (A-Beta+(TTR+KPI−−APP)) did not affected TTR activity (lower panels). Scale bar=500 nm.
Neuromics' Reagent Used-APP 228
MMP-9, E. Coli and Breast Cancer
Interestingly, the authors observed a postive change in the expression of these proteins after colonization.
Stephanie Weibel, Jochen Stritzker, Matthias Eck, Werner Goebel, and Aladar A. Szalay. Colonization of experimental murine breast tumours by Escherichia coli K-12 significantly alters the tumour microenvironment. 10.1111/j.1462-5822.2008.01122.x. Cellular Microbiology. © 2008 Blackwell Publishing Ltd
...goat anti-mouse MMP-9 antibody (Neuromics, Edina, MN)...
Thursday, August 14, 2008
Monday, August 11, 2008
Cholesterol Homeostasis and Diabetes
Scientists have also shown that pancreatic beta cells, responsible for insulin release, begin to malfunction when their cholesterol levels build up. So what is the link?
The study referenced here suggests that HSL plays a critical role in the hydrolysis of cytosolic cholesteryl esters and that increased levels of hepatic cholesteryl esters, due to lack of action of HSL in the liver, is the main mechanism underlying the imbalance in cholesterol metabolism in HSL-null mice.
Celine Fernandez, Marie Lindholm, Morten Krogh, Stéphanie Lucas, Sara Larsson, Peter Osmark, Karin Berger, Jan Boren, Barbara A Fielding, Keith N. Frayn and Cecilia Holm. Disturbed cholesterol homeostasis in hormone-sensitive lipase null mice. Am J Physiol Endocrinol Metab (July 29, 2008). doi:10.1152/ajpendo.90206.2008.
...Liver samples were homogenized in lysis buffer pH 7.0 containing 25 mM Tris, 150 mM NaCl, 1 mM EDTA, 1% Triton and 1X protease inhibitor cocktail (Complete Mini, Roche). Total protein concentration was measured by BCA assay (Pierce) and 50 μg of protein were subjected to SDS-polyacrylamide gel electrophoresis (8 % polyacrylamide). After transfer to PVDF membranes (Invitrogen), blots were incubated with a primary antibody mouse anti-mouse/rat ABCA1 (Neuromics) according to the instructionsof the manufacturer. As secondary antibody a horseradish peroxidase-conjugated sheep antimouse IgG was used. Western blot analysis was performed using a chemiluminescence system (Luminol) and detection was made using a CCD-camera (LAS 1000, Fuji). Band intensities were quantified using the ImageJ software (http://rsb.info.nih.gov/ij)...
MMP-9 and Neuroinflammation & Autoimmunity
... Metalloproteinase 9 (MMP-9); 1:500; Neuromics, Edina, MN, USA...
Related Reagents:
proMMP-7 (Human)
MMP-24 (MT5-MMP, Human)
Cancer Antibodies
Neurodegenerative Disease Antibodies
Pain and Inflammation
Thursday, August 07, 2008
New Neurotensin Receptor (NTS-1) antibody
Tuesday, August 05, 2008
TRPV1 Staining of Mouse DRG
This excellent staining comes to us courtesy of Katharina Zimmermann (Childrens Hospital Boston, Clapham Lab). This is some of the best staining we've seen using our VR1 C-Terminus (TRPV1) - mouse specific antibody.Images: TRPV1 staining of C57BL/6 mouse dorrsal root ganglia. Tissues were stained using Alexa Fluor© 488 (Green) and counterstained with DAPI (blue).
cryosections, 10 microns thickness

