钾离子通道蛋白家族成员1样蛋白抗体
规格：1mg/1ml
英文名： KCNE1L
别名： AMME syndrome candidate gene 2 protein; AMMECR2 protein; Cardiac voltage gated potassium channel accessory subunit 5; KCNE1 like; KCNE5; Mink; MinK like protein; Potassium voltage gated channel subfam
分子量： 15kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：Polyclonal
亚型：IgG
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human KCNE1L
交叉反应：Human, Mouse, Rat, Pig, Cow, Rabbit, Sheep,
细胞定位：细胞浆 细胞膜
钾离子通道蛋白家族成员1样蛋白抗体产品介绍：background: KCNE1L belongs to the potassium channel KCNE family which represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Subcellular Location: Plasma membrane; Single-pass type I membrane protein. Tissue Specificity: Highly 钾离子通道蛋白家族成员1样蛋白抗体expressed in heart, skeletal muscle, brain, spinal cord and placenta. DISEASE: Defects in KCNE1L are involved in Alport syndrome with mental retardation midface hypoplasia and elliptocytosis (ATS-MR) [MIM:300194]. A X-linked contiguous gene deletion syndrome characterized by glomerulonephritis, deafness, mental retardation, midface hypoplasia and elliptocytosis. Similarity: Belongs to the potassium钾离子通道蛋白家族成员1样蛋白抗体 channel KCNE family. Database links: Entrez Gene: 23630 Human Omim: 300328 Human SwissProt: Q9UJ90 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产钾离子通道蛋白家族成员1样蛋白抗体品应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 （石蜡切片需做抗原修复） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
研究领域：心血管 神经生物学 通道蛋白
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid