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Rho-related GTP-binding protein 抗体 (C-Term)

The 兔 多克隆 anti-Rho-related GTP-binding protein antibody is suitable to detect Rho-related GTP-binding protein in samples from 人, 大鼠 和 小鼠. It has been validated for WB.
产品编号 ABIN1537109
发货至: 中国
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Quick Overview for Rho-related GTP-binding protein 抗体 (C-Term) (ABIN1537109)

抗原

See all Rho-related GTP-binding protein (RhO (pan)) 抗体
Rho-related GTP-binding protein (RhO (pan))

适用

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人, 大鼠, 小鼠

宿主

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克隆类型

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多克隆

标记

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This Rho-related GTP-binding protein antibody is un-conjugated

应用范围

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Western Blotting (WB)

克隆位点

RB36659
  • 抗原表位

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    AA 310-339, C-Term

    预测反应

    Pr

    纯化方法

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

    免疫原

    This RHO antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 310-339 amino acids from the C-terminal region of human RHO.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:2000. 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

    RHO Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    有效期

    6 months
  • 抗原

    Rho-related GTP-binding protein (RhO (pan))

    别名

    RHO

    物质类

    Chemical

    背景

    Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.

    分子量

    38893

    基因ID

    6010

    NCBI登录号

    NP_000530

    UniProt

    P08100
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