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CCDC148 抗体 (AA 401-500) (Cy3)

This anti-CCDC148 antibody is a 兔 多克隆 antibody detecting CCDC148 in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN887328
发货至: 中国

Quick Overview for CCDC148 抗体 (AA 401-500) (Cy3) (ABIN887328)

抗原

See all CCDC148 抗体
CCDC148 (Coiled-Coil Domain Containing 148 (CCDC148))

适用

  • 25
  • 8

宿主

  • 23
  • 2

克隆类型

  • 25
多克隆

标记

  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CCDC148 antibody is conjugated to Cy3

应用范围

  • 25
  • 12
  • 12
  • 10
  • 9
  • 3
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 401-500

    预测反应

    Human,Mouse,Rat,Cow,Sheep,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CCDC148

    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

    CCDC148 (Coiled-Coil Domain Containing 148 (CCDC148))

    别名

    CCDC148

    背景

    Synonyms: CCDC 148, coiled coil domain containing 148, coiled-coil domain containing 148, CC148_HUMAN.

    Background: CCDC148 (coiled-coil domain containing 148), also known as MGC125590 or MGC125588, is a 591 amino acid protein encoded by a gene mapping to human chromosome 2. The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

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