Trpm7 monoclonal antibody, clone S74-25
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More Files
- More Functions
Western Blot (Cell lysate)
Western blot analysis of human cell line mixed lysate with Trpm7 monoclonal antibody, clone S74-25 (Cat # MAB6663).
Immunofluorescence
Immunofluorescence staining in human hippocampus with Trpm7 monoclonal antibody, clone S74-25 (Cat # MAB6663).
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Specification
Product Description
Mouse monoclonal antibody raised against partial recombinant Trpm7.
Immunogen
Recombinant fusion protein corresponding to C-terminus amino acids 1817-1863 of mouse Trpm7.
Host
Mouse
Reactivity
Human, Mouse, Rat
Specificity
Detects ~220KDa. No cross-reactivity against TrpM6.
Form
Liquid
Isotype
IgG1
Recommend Usage
Western Blot (1-10 ug/mL)
Immunohistochemistry (0.1-1.0 ug/mL)
Immunocytochemistry (0.1-1.0 ug/mL)
Immunofluorescence (1.0-10 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.4 (50% glycerol, 0.09% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western blot analysis of human cell line mixed lysate with Trpm7 monoclonal antibody, clone S74-25 (Cat # MAB6663).Immunocytochemistry
Immunofluorescence
Immunofluorescence staining in human hippocampus with Trpm7 monoclonal antibody, clone S74-25 (Cat # MAB6663).Immunoprecipitation
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Gene Info — Trpm7
Entrez GeneID
58800Protein Accession#
Q923J1Gene Name
Trpm7
Gene Alias
2310022G15Rik, 4833414K03Rik, 5033407O22Rik, CHAK, CHAK1, Ltpr7, Ltrpc7, TRP-PLIK
Gene Description
transient receptor potential cation channel, subfamily M, member 7
Gene Ontology
HyperlinkGene Summary
subfamily M
Other Designations
OTTMUSP00000017028|transient receptor potential M7|transient receptor potential-related protein, ChaK
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Publication Reference
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Congenital long QT syndrome.
Crotti L, Celano G, Dagradi F, Schwartz PJ.
Orphanet Journal of Rare Diseases 2008 Jul; 3:18.
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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Splawski I, Timothy KW, Sharpe LM, Decher N, Kumar P, Bloise R, Napolitano C, Schwartz PJ, Joseph RM, Condouris K, Tager-Flusberg H, Priori SG, Sanguinetti MC, Keating MT.
Cell 2004 Oct; 119(1):19.
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Congenital long QT syndrome.
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