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LearnNB500-242
antibody from Novus Biologicals
Targeting: TRPM2
EREG1, KNP3, LTRPC2, NUDT9H, NUDT9L1, TRPC7
Western blot
ImmunocytochemistryAntibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations
- Western blot [1]
- Immunoprecipitation [1]
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- Product number
- NB500-242 - Provider product page
- Provider
- Novus Biologicals
- Proper citation
- Novus Cat#NB500-242, RRID:AB_10002013
- Product name
- Rabbit Polyclonal TRPM2 Antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified.
- Reactivity
- Human, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 ul
- Concentration
- 1.0 mg/ml
- Storage
- Store at 4C. Do not freeze.
Submitted references Expression and functional properties of TRPM2 channels in dopaminergic neurons of the substantia nigra of the rat.
Ca2+-dependent induction of TRPM2 currents in hippocampal neurons.
Sphingosine kinase 1 is up-regulated during hypoxia in U87MG glioma cells. Role of hypoxia-inducible factors 1 and 2.
Chemotaxis of mouse bone marrow neutrophils and dendritic cells is controlled by adp-ribose, the major product generated by the CD38 enzyme reaction.
Chemotaxis of mouse bone marrow neutrophils and dendritic cells is controlled by adp-ribose, the major product generated by the CD38 enzyme reaction.
Chung KK, Freestone PS, Lipski J
Journal of neurophysiology 2011 Dec;106(6):2865-75
Journal of neurophysiology 2011 Dec;106(6):2865-75
Ca2+-dependent induction of TRPM2 currents in hippocampal neurons.
Olah ME, Jackson MF, Li H, Perez Y, Sun HS, Kiyonaka S, Mori Y, Tymianski M, MacDonald JF
The Journal of physiology 2009 Mar 1;587(Pt 5):965-79
The Journal of physiology 2009 Mar 1;587(Pt 5):965-79
Sphingosine kinase 1 is up-regulated during hypoxia in U87MG glioma cells. Role of hypoxia-inducible factors 1 and 2.
Anelli V, Gault CR, Cheng AB, Obeid LM
The Journal of biological chemistry 2008 Feb 8;283(6):3365-75
The Journal of biological chemistry 2008 Feb 8;283(6):3365-75
Chemotaxis of mouse bone marrow neutrophils and dendritic cells is controlled by adp-ribose, the major product generated by the CD38 enzyme reaction.
Partida-Sanchez S, Gasser A, Fliegert R, Siebrands CC, Dammermann W, Shi G, Mousseau BJ, Sumoza-Toledo A, Bhagat H, Walseth TF, Guse AH, Lund FE
Journal of immunology (Baltimore, Md. : 1950) 2007 Dec 1;179(11):7827-39
Journal of immunology (Baltimore, Md. : 1950) 2007 Dec 1;179(11):7827-39
Chemotaxis of mouse bone marrow neutrophils and dendritic cells is controlled by adp-ribose, the major product generated by the CD38 enzyme reaction.
Partida-Sanchez S, Gasser A, Fliegert R, Siebrands CC, Dammermann W, Shi G, Mousseau BJ, Sumoza-Toledo A, Bhagat H, Walseth TF, Guse AH, Lund FE
Journal of immunology (Baltimore, Md. : 1950) 2007 Dec 1;179(11):7827-39
Journal of immunology (Baltimore, Md. : 1950) 2007 Dec 1;179(11):7827-39
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Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Western Blot: TRPM2 Antibody [NB500-242] - Samples: Jurkat Membrane Prep (50, 15, 5 ug). Antibody: Affinity purified rabbit anti-TRPM2 antibody used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.
Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Immunoprecipitation: TRPM2 Antibody [NB500-242] - Samples: Membrane Prep (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from Jurkat cells. Antibodies: Affinity purified rabbit anti-TRPM2 antibody NB500-242 used for IP at 6 ug per reaction. TRPM2 was also immunoprecipitated by rabbit anti-TRPM2 antibody NB500-241. For blotting immunoprecipitated TRPM2, NB500-242 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.
