Product Name	Recombinant Rabbit Anti-Kcnj6 Monoclonal Antibody
Cat No.	SLA1079M
Chinese Name	G蛋白激活内流钾通道蛋白2重组兔单克隆抗体
Alias	BIR1; GIRK-2; GIRK2; KATP-2; KATP2; KCNJ7; KIR3.2; KPLBS; hiGIRK2; weaver; wv; KCNJ6_HUMAN; KCNJ6; Inward rectifier K(+) channel Kir3.2; Potassium channel, inwardly rectifying subfamily J member 6; KCNJ6_MOUSE; W; KCNJ6_RAT; potassium inwardly rectifying channel subfamily J member 6; potassium inwardly-rectifying channel, subfamily J, member 6; G protein-activated inward rectifier potassium channel 2
Host Species	Rabbit
Isotype	IgG
Clonality	Monoclonal
React Species	Mouse
Applications	WB (1:500-2000) Not yet tested in other applications. Optimal working dilutions must be determined by the end user.
Immunogen	KLH conjugated synthetic peptide derived from mouse KCNJ6
Purification	affinity purified by Protein A
Concentration	1mg/ml
Predicted MW.	47 kDa
Observed MW.	40, 48 kDa
Gene ID	16522
Swiss-Prot	P48542
Storage	0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Background	This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.