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PROSER2 抗体 (Biotin)

PROSER2 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1404553
发货至: 中国
  • 抗原 See all PROSER2 products
    PROSER2 (Proline and Serine-Rich Protein 2 (PROSER2))
    适用
    • 20
    • 18
    • 18
    • 4
    人, 小鼠, 大鼠
    宿主
    • 20
    克隆类型
    • 20
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PROSER2 antibody is conjugated to Biotin
    应用范围
    • 20
    • 13
    • 2
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C10orf47
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    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 for 12 months.
    有效期
    12 months
  • 抗原
    PROSER2 (Proline and Serine-Rich Protein 2 (PROSER2))
    别名
    C10orf47 (PROSER2 产品)
    别名
    C10orf47 antibody, proline and serine rich 2 antibody, PROSER2 antibody
    背景

    Synonyms: C10orf47, Chromosome 10 open reading frame 47, CJ047_HUMAN, Hypothetical protein LOC254427, MGC35403, Uncharacterized protein C10orf47.

    Background: C10orf47 is a 435 amino acid protein that exists as two alternatively spliced isoforms that are encoded by a gene located on human chromosome 10. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

    基因ID
    254427
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