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GLRB 抗体 (N-Term)

This anti-GLRB antibody is a 兔 多克隆 antibody detecting GLRB in WB. Suitable for 人.
产品编号 ABIN5536519
发货至: 中国

Quick Overview for GLRB 抗体 (N-Term) (ABIN5536519)

抗原

See all GLRB 抗体
GLRB (Glycine Receptor, beta (GLRB))

适用

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宿主

  • 40
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克隆类型

  • 40
  • 1
多克隆

标记

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This GLRB antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    AA 103-132, N-Term

    纯化方法

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

    免疫原

    This GLRB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 103-132 amino acids from the N-terminal region of human GLRB.

    亚型

    Ig Fraction
  • 应用备注

    For WB starting dilution is: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5 mg/mL

    缓冲液

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • 抗原

    GLRB (Glycine Receptor, beta (GLRB))

    别名

    GLRB

    背景

    This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants.

    分子量

    56 kDa

    基因ID

    2743

    UniProt

    P48167
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