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Recombinant PMS2 抗体 (AA 1-100)

The 兔 单克隆 anti-PMS2 antibody (Clone PMS2-4373R) (ABIN7867882) specifically detects PMS2 in IHC (p). The antibody is reactive with 人 samples.
产品编号 ABIN7867882
发货至: 中国
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Quick Overview for Recombinant PMS2 抗体 (AA 1-100) (ABIN7867882)

抗原

See all PMS2 抗体
PMS2 (PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae) (PMS2))

抗体类型

Recombinant Antibody

适用

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宿主

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克隆类型

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单克隆

标记

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This PMS2 antibody is un-conjugated

应用范围

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Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

PMS2-4373R
  • 抗原表位

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    AA 1-100

    原理

    Recombinant PMS2 Antibody / PMS1 homolog 2

    纯化方法

    Protein A affinity chromatography

    免疫原

    A portion of amino acids 1-100 from the human protein was used as the immunogen for the recombinant PMS2 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the recombinant PMS2 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.2 mg/mL

    缓冲液

    0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced) and 0.05 % 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 the recombinant PMS2 antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • 抗原

    PMS2 (PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae) (PMS2))

    别名

    PMS2

    背景

    PMS2 is involved in DNA mismatch repair. It forms a heterodimer with MLH1 and this complex interacts with other complexes bound to mismatched bases. Defects in PMS2 are the cause of hereditary non-polyposis colorectal cancer type 4 (HNPCC4). Mutations in more than one gene locus can be involved alone or in combination in the production of the HNPCC phenotype (also called Lynch syndrome). Most families with clinically recognized HNPCC have mutations in either MLH1 or MSH2 genes. HNPCC is an autosomal, dominantly inherited disease associated with marked increase in cancer susceptibility. It is characterized by a familial predisposition to early onset colorectal carcinoma (CRC) and extra-colonic cancers of the gastrointestinal, urological and female reproductive tracts. HNPCC is reported to be the most common form of inherited colorectal cancer in the Western world, and accounts for 15 % of all colon cancers. Defects in PMS2 are a cause of mismatch repair cancer syndrome (MMRCS), also known as Turcot syndrome or brain tumor-polyposis syndrome 1 (BTPS1). MMRCS is an autosomal dominant disorder characterized by malignant tumors of the brain associated with multiple colorectal adenomas. Skin features include sebaceous cysts, hyperpigmented and cafe au lait spots.

    UniProt

    P54278

    途径

    DNA Damage Repair, Production of Molecular Mediator of Immune Response
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