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CCDC104 抗体 (AA 241-342)

This anti-CCDC104 antibody is a 兔 多克隆 antibody detecting CCDC104 in ELISA, IF (cc), IF (p), IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN872777
发货至: 中国

Quick Overview for CCDC104 抗体 (AA 241-342) (ABIN872777)

抗原

See all CCDC104 抗体
CCDC104 (Coiled-Coil Domain Containing 104 (CCDC104))

适用

  • 1
  • 1

宿主

  • 1

克隆类型

  • 1
多克隆

标记

  • 1
This CCDC104 antibody is un-conjugated

应用范围

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

    AA 241-342

    预测反应

    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CCDC104

    亚型

    IgG
  • 应用备注

    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

    CCDC104 (Coiled-Coil Domain Containing 104 (CCDC104))

    别名

    CCDC104

    背景

    Synonyms: CC104_HUMAN, CCDC104, Coiled coil domain containing 104, Coiled-coil domain-containing protein 104, MGC15407.

    Background: CCDC104 is a 342 amino acid protein that exists as two alternatively spliced isoforms. CCDC104 undergoes post-translational phosphorylation following DNA damage, most likely by either ATR or ATM. The gene encoding CCDC104 maps to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes 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.

    基因ID

    112942
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