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KLHDC8A 抗体 (AA 51-150) (Cy5)

This anti-KLHDC8A antibody is a 兔 多克隆 antibody detecting KLHDC8A in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1416486
发货至: 中国

Quick Overview for KLHDC8A 抗体 (AA 51-150) (Cy5) (ABIN1416486)

抗原

See all KLHDC8A 抗体
KLHDC8A (Kelch Domain Containing 8A (KLHDC8A))

适用

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宿主

  • 27

克隆类型

  • 27
多克隆

标记

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This KLHDC8A antibody is conjugated to Cy5

应用范围

  • 22
  • 12
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  • 10
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 4
    • 1
    AA 51-150

    预测反应

    Human,Mouse,Rat,Cow,Pig,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human KLHDC8A

    亚型

    IgG
  • 应用备注

    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

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    KLHDC8A (Kelch Domain Containing 8A (KLHDC8A))

    别名

    KLHDC8A

    背景

    Synonyms: Kelch domain containing 8A, Kelch domain containing protein 8A, KLHDC 8A, MGC19056, RGD1305132, A630065K24Rik, FLJ10748, KLD8A_HUMAN.

    Background: Kelch domain-containing protein 8A (KLHDC8A) is a 350 amino acid protein. KLHDC8A contains seven kelch repeats, each of which is an approximately 50 amino acid long conserved region that forms a tertiary structure beta-propeller. The gene that encodes KLHDC8A is located on chromosome 1, which is the largest human chromosome, spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes Lamin A. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    基因ID

    55220
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