Kcnj2 monoclonal antibody, clone S112
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Specification
Product Description
Mouse monoclonal antibody raised against synthetic peptide of Kcnj2.
Immunogen
A synthetic peptide corresponding to amino acids 390-411 of mouse Kcnj2.
Host
Mouse
Reactivity
Mouse, Rat
Specificity
Detects ~55KDa. No cross-reactivity against Kir2.2 or Kir2.3.
Form
Liquid
Isotype
IgG1
Recommend Usage
Western Blot (1-10 ug/mL)
Immunocytochemistry (0.1-1.0 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
Immunocytochemistry
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Gene Info — Kcnj2
Entrez GeneID
16518Protein Accession#
NP_032451Gene Name
Kcnj2
Gene Alias
IRK1, Kcnf1, Kir2.1
Gene Description
potassium inwardly-rectifying channel, subfamily J, member 2
Gene Ontology
HyperlinkGene Summary
subfamily J
Other Designations
OTTMUSP00000003316|potassium inwardly-rectifying channel J2
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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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