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FAM153B 抗体 (AA 301-387)

This anti-FAM153B antibody is a 兔 多克隆 antibody detecting FAM153B in WB, ELISA, IF (cc), IF (p), IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN872845
发货至: 中国

Quick Overview for FAM153B 抗体 (AA 301-387) (ABIN872845)

抗原

FAM153B (Family with Sequence Similarity 153, Member B (FAM153B))

适用

宿主

  • 4

克隆类型

  • 4
多克隆

标记

  • 4
This FAM153B antibody is un-conjugated

应用范围

Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 1
    • 1
    • 1
    • 1
    AA 301-387

    交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human FAM153B

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    FAM153B (Family with Sequence Similarity 153, Member B (FAM153B))

    别名

    Fam153b

    背景

    Synonyms: DKFZp434D115, F153B_HUMAN, FAM153B, Family with sequence similarity 153, member B, Hypothetical protein LOC202134, OTTHUMP00000223257, Protein FAM153B.

    Background: FAM153A, FAM153B and FAM153C are 310, 387 and 144 amino acid proteins, respectively, that are encoded by a genes mapping to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

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