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Bestrophin 1 抗体

This anti-Bestrophin 1 antibody is a 兔 多克隆 antibody detecting Bestrophin 1 in WB. Suitable for 人.
产品编号 ABIN2854513
发货至: 中国

Quick Overview for Bestrophin 1 抗体 (ABIN2854513)

抗原

See all Bestrophin 1 (BEST1) 抗体
Bestrophin 1 (BEST1)

适用

  • 23
  • 4
  • 3
  • 2
  • 2
  • 1

宿主

  • 21
  • 4

克隆类型

  • 23
  • 2
多克隆

标记

  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Bestrophin 1 antibody is un-conjugated

应用范围

  • 17
  • 8
  • 7
  • 5
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB)
  • 交叉反应

    产品特性

    Rabbit Polyclonal antibody to Bestrophin 1 (bestrophin 1)
    Bestrophin 1 antibody

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human Bestrophin 1. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: NT2D1 , PC-3 , SK-N-SH

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Bestrophin 1 (BEST1)

    别名

    bestrophin 1

    背景

    This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.

    Cellular Localization: Cell membrane

    分子量

    68 kDa

    基因ID

    7439

    UniProt

    O76090
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