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CCDC125 抗体 (AA 151-250) (Alexa Fluor 647)

CCDC125 适用: 小鼠 WB, IF (cc), IF (p) 宿主: 兔 Polyclonal Alexa Fluor 647
产品编号 ABIN887124
发货至: 中国
  • 抗原 See all CCDC125 抗体
    CCDC125 (Coiled-Coil Domain Containing 125 (CCDC125))
    抗原表位
    AA 151-250
    适用
    • 14
    • 1
    小鼠
    宿主
    • 15
    克隆类型
    • 15
    多克隆
    标记
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CCDC125 antibody is conjugated to Alexa Fluor 647
    应用范围
    • 15
    • 12
    • 12
    • 4
    • 3
    • 3
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    小鼠
    预测反应
    Human,Rat,Cow,Sheep,Pig
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human CCDC125
    亚型
    IgG
    Top Product
    Discover our top product CCDC125 Primary Antibody
  • 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
    CCDC125 (Coiled-Coil Domain Containing 125 (CCDC125))
    别名
    CCDC125 (CCDC125 产品)
    别名
    KENAE antibody, 5830436D01Rik antibody, AL023012 antibody, Kenae-like antibody, RGD1561673 antibody, si:ch211-214j8.8 antibody, coiled-coil domain containing 125 antibody, CCDC125 antibody, Ccdc125 antibody, ccdc125 antibody
    背景

    Synonyms: CC125_HUMAN, CCDC125, Coiled-coil domain-containing protein 125, KENAE,y Protein kenae.

    Background: CCDC125, also known as KENAE, is a 511 amino acid protein expressed as two isoforms produced by alternative splicing and encoded by a gene 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.

    基因ID
    202243
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