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DENND2C 抗体

DENND2C 适用: 人, 小鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385606
发货至: 中国
  • 抗原 See all DENND2C products
    DENND2C (DENN/MADD Domain Containing 2C (DENND2C))
    适用
    • 22
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    人, 小鼠
    宿主
    • 22
    克隆类型
    • 22
    多克隆
    标记
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    • 1
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    This DENND2C antibody is un-conjugated
    应用范围
    • 18
    • 12
    • 5
    • 2
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human DENND2C
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 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
    DENND2C (DENN/MADD Domain Containing 2C (DENND2C))
    别名
    DENND2C (DENND2C 产品)
    别名
    si:dkeyp-46c9.6 antibody, MGC145874 antibody, dJ1156J9.1 antibody, A930010I20Rik antibody, RGD1308197 antibody, DENN domain containing 2C antibody, DENN/MADD domain containing 2C antibody, DENND2C antibody, dennd2c antibody, Dennd2c antibody
    背景

    Synonyms: DENN/MADD domain containing 2C, dJ1156J9.1, DKFZp686G0351, DKFZp686N1631, DKFZp779P1149, FLJ37099, RP5-1156J9.1, DEN2C_HUMAN.

    Background: DENND2C is a 928 amino acid protein that contains a dDENN domain, a DENN domain, and a uDENN domain and exists as three isoforms as a result of alternative splicing. The DENND2C protein is thought to target to actin filaments and control Rab9-dependent trafficking of mannose-6-phosphate receptor to lysosomes. The gene encoding DENND2C maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.

    基因ID
    163259
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