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Bestrophin 1 抗体 (DyLight 488)

BEST1 适用: 人 FACS 宿主: 兔 Polyclonal DyLight 488
产品编号 ABIN7354625
发货至: 中国
  • 抗原 See all Bestrophin 1 (BEST1) 抗体
    Bestrophin 1 (BEST1)
    适用
    • 22
    • 4
    • 3
    • 2
    • 2
    • 1
    宿主
    • 19
    • 4
    克隆类型
    • 21
    • 2
    多克隆
    标记
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Bestrophin 1 antibody is conjugated to DyLight 488
    应用范围
    • 16
    • 7
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Flow Cytometry (FACS)
    序列
    RFIYRLALTE EQQLMFEKLT LYCD
    交叉反应 (详细)
    No cross reactivity with other proteins.
    产品特性
    Rabbit IgG Polyclonal Anti-Human Bestrophin Antibody DyLight® 488 Conjugated, Flow Validated.
    免疫原
    A synthetic peptide corresponding to a sequence of human Bestrophin (RFIYRLALTEEQQLMFEKLTLYCD).
    Top Product
    Discover our top product BEST1 Primary Antibody
  • 应用备注

    Application Details: Flow Cytometry, 1-3 μg/1x106 cells

    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg NaN3.
    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
    储存方法
    At 2-8°C for one year. Protect from light. Do not freeze.
  • 抗原
    Bestrophin 1 (BEST1)
    别名
    BEST1 (BEST1 产品)
    背景

    Synonyms: Bestrophin-1, TU15B, Vitelliform macular dystrophy protein 2, BEST1, VMD2

    Tissue Specificity: Predominantly expressed in the basolateral membrane of the retinal pigment epithelium.

    Background: Bestrophin-1 (Best1) is a protein that, in humans, is encoded by the BEST1 gene. 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.

    UniProt
    O76090
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