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CCDC148 抗体 (AA 401-500) (AbBy Fluor® 594)

CCDC148 适用: 人 WB, IF (p), IF (cc) 宿主: 兔 Polyclonal AbBy Fluor® 594
产品编号 ABIN2811205
发货至: 中国
  • 抗原 See all CCDC148 抗体
    CCDC148 (Coiled-Coil Domain Containing 148 (CCDC148))
    抗原表位
    • 14
    • 7
    • 7
    • 6
    • 6
    • 2
    • 1
    AA 401-500
    适用
    • 30
    • 8
    宿主
    • 28
    • 2
    克隆类型
    • 30
    多克隆
    标记
    • 7
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CCDC148 antibody is conjugated to AbBy Fluor® 594
    应用范围
    • 30
    • 15
    • 13
    • 12
    • 12
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
    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
    Top Product
    Discover our top product CCDC148 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
    CCDC148 (Coiled-Coil Domain Containing 148 (CCDC148))
    别名
    CCDC148 (CCDC148 产品)
    别名
    5830402J09 antibody, RGD1561169 antibody, coiled-coil domain containing 148 antibody, CCDC148 antibody, Ccdc148 antibody
    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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