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KIR2.1 Polyclonal Antibody

说明书

BYab-16441

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
WB;IHC;IF;ELISA
分子量(DA)
48kD
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.
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
稀释比例
WB: 1/500 - 1/2000. IHC: 1/100 - 1/300. ELISA: 1/10000.. IF 1:50-200
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度
1 mg/ml
背景(Background)
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],
功能
disease:Defects in KCNJ2 are the cause of long QT syndrome type 7 (LQT7) [MIM:170390]; also called Andersen syndrome or Andersen cardiodysrhythmic periodic paralysis. Long QT syndromes are heart disorders characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. They cause syncope and sudden death in response to excercise or emotional stress. LQT7 manifests itself as a clinical triad consisting of potassium-sensitive periodic paralysis, ventricular ectopy and dysmorphic features.,disease:Defects in KCNJ2 are the cause of short QT syndrome type 3 (SQT3) [MIM:609622]. Short QT syndromes are heart disorders characterized by idiopathic persistently and uniformly short QT interval on ECG in the absence of structural heart disease in affected individuals. They cause syncope and sudden death. SQT3 has a unique ECG phenotype characterized by asymmetrical T wave
基因名称(Gene Name)
KCNJ2
蛋白名称
Inward rectifier potassium channel 2
简称
KIR2.1
其他名称
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
Fields
>>Cholinergic synapse;>>Oxytocin signaling pathway;>>Renin secretion;>>Gastric acid secretion
人基因ID
3759
人蛋白质序列数据库
P63252
小鼠基因ID
小鼠蛋白质序列数据库
P35561
大鼠基因ID
29712
大鼠蛋白质序列数据库
Q64273
细胞定位
Membrane; Multi-pass membrane protein. Membrane; Lipid-anchor .
组织表达
Heart, brain, placenta, lung, skeletal muscle, and kidney. Diffusely distributed throughout the brain.
储存(Storage)
-20°C/1 year

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KIR2.1 Polyclonal Antibody

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