- 产品信息
商品描述
靶点-Target
KIR2.1
反应性
Human,Rat
应用
WB,IHC,IF,ELISA
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Observed)
48kD
推荐稀释比
WB 1:500-1:2000;IHC 1:100-1:300;ELISA 1:10000;IF 1:50-200
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
克隆性
Polyclonal
免疫原
The antiserum was produced against synthesized peptide derived from human KCNJ2. AA range:81-130
特异性
KIR2.1 Polyclonal Antibody detects endogenous levels of KIR2.1 protein.
基因名称
KCNJ2
蛋白名称
Inward rectifier potassium channel 2
别名
KCNJ2;IRK1;Inward rectifier potassium channel 2;Cardiac inward rectifier potassium channel;Inward rectifier K;+;channel Kir2.1;IRK-1;hIRK1;Potassium channel;inwardly rectifying subfamily J member 2
Organism-1
Human
基因ID-1
3759
SwissProt-1
P63252
Organism-2
Mouse
SwissProt-2
P35561
Organism-3
Rat
基因ID-3
29712
SwissProt-3
Q64273
背景
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008],
细胞定位
Membrane; Multi-pass membrane protein. Membrane; Lipid-anchor .





