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KIAA1522 抗体 (AA 101-250)

KIAA1522 适用: 人 WB, ELISA, ICC, IF (cc), IF (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1387607
发货至: 中国
  • 抗原 See all KIAA1522 products
    KIAA1522
    抗原表位
    • 1
    • 1
    AA 101-250
    适用
    • 2
    • 1
    • 1
    • 1
    宿主
    • 2
    克隆类型
    • 2
    多克隆
    标记
    • 2
    This KIAA1522 antibody is un-conjugated
    应用范围
    Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    交叉反应
    预测反应
    Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human KIAA1522
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    ELISA 1:500-1000
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500
    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
  • Liu, Yang, Cao, Jiang, Hao, Xu, Cai, Wang: "KIAA1522 is a novel prognostic biomarker in patients with non-small cell lung cancer." in: Scientific reports, Vol. 6, pp. 24786, (2017) (PubMed).

  • 抗原
    KIAA1522
    别名
    KIAA1522 (KIAA1522 产品)
    别名
    Kiaa1522 antibody, mKIAA1522 antibody, expressed sequence C77080 antibody, KIAA1522 antibody, KIAA1522 ortholog antibody, C77080 antibody, KIAA1522 antibody
    背景

    Synonyms: K1522_HUMAN, Kiaa1522, Uncharacterized protein KIAA1522.

    Background: KIAA1522 is a 1,035 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 1p35.1. Chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

    基因ID
    57648
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