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RRBP1 抗体

The 兔 多克隆 anti-RRBP1 antibody (ABIN7882178) specifically detects RRBP1 in WB, FACS, IF, IHC (p) 和 ICC. The antibody is reactive with 人 samples.
产品编号 ABIN7882178
发货至: 中国
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Quick Overview for RRBP1 抗体 (ABIN7882178)

抗原

See all RRBP1 抗体
RRBP1 (Ribosome Binding Protein 1 (RRBP1))

适用

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宿主

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克隆类型

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多克隆

标记

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This RRBP1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
  • 原理

    RRBP1 Antibody / Ribosome binding protein 1

    序列

    EKEKKLTSDL GRAATRLQEL LKTTQEQLAR EKDTVKKLQE QLEKAED

    纯化方法

    Antigen affinity purified

    免疫原

    Amino acids EKEKKLTSDLGRAATRLQELLKTTQEQLAREKDTVKKLQEQLEKAED from the human protein were used as the immunogen for the RRBP1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the RRBP1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the RRBP1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    RRBP1 (Ribosome Binding Protein 1 (RRBP1))

    别名

    RRBP1

    背景

    Ribosome-binding protein 1, also referred to as p180, is a protein that in humans is encoded by the RRBP1 gene. It is mapped to 20p12.1. This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12.

    UniProt

    Q9P2E9
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