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KCNE1-Like 抗体 (AA 67-96)

This anti-KCNE1-Like antibody is a 兔 多克隆 antibody detecting KCNE1-Like in WB. Suitable for 人.
产品编号 ABIN653619
发货至: 中国

Quick Overview for KCNE1-Like 抗体 (AA 67-96) (ABIN653619)

抗原

See all KCNE1-Like (KCNE1L) 抗体
KCNE1-Like (KCNE1L)

适用

  • 28
  • 17
  • 16
  • 1
  • 1

宿主

  • 28

克隆类型

  • 28
多克隆

标记

  • 9
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KCNE1-Like antibody is un-conjugated

应用范围

  • 28
  • 13
  • 9
  • 4
  • 1
  • 1
Western Blotting (WB)

克隆位点

RB24387
  • 抗原表位

    • 7
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 67-96

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This KCE1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 67-96 amino acids from the Central region of human KCE1L.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    KCNE1-Like (KCNE1L)

    别名

    KCE1L

    背景

    Voltage-gated potassium (Kv) channels 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. This gene encodes a membrane protein which has sequence similarity to the KCNE1 gene product, a member of the potassium channel, voltage-gated, isk-related subfamily. This intronless gene is deleted in AMME contiguous gene syndrome and may be involved in the cardiac and neurologic abnormalities found in the AMME contiguous gene syndrome.

    分子量

    14993

    基因ID

    23630

    NCBI登录号

    NP_036414

    UniProt

    Q9UJ90
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