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ASCC2 抗体

ASCC2 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7242971
发货至: 中国
  • 抗原 See all ASCC2 抗体
    ASCC2 (Activating Signal Cointegrator 1 Complex Subunit 2 (ASCC2))
    适用
    • 24
    • 12
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 16
    • 8
    克隆类型
    • 19
    • 5
    多克隆
    标记
    • 17
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ASCC2 antibody is un-conjugated
    应用范围
    • 17
    • 6
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human ASCC2
    亚型
    IgG
    Top Product
    Discover our top product ASCC2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.7 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
  • 抗原
    ASCC2 (Activating Signal Cointegrator 1 Complex Subunit 2 (ASCC2))
    别名
    ASCC2 (ASCC2 产品)
    别名
    MGC63666 antibody, zgc:63666 antibody, ASCC2 antibody, ascc2 antibody, asc1p100 antibody, ASC1p100 antibody, p100 antibody, 1700011I11Rik antibody, 2610034L15Rik antibody, AI482016 antibody, AW046480 antibody, RGD1561422 antibody, activating signal cointegrator 1 complex subunit 2 antibody, activating signal cointegrator 1 complex subunit 2 S homeolog antibody, ascc2 antibody, ASCC2 antibody, MCYG_08331 antibody, ascc2.S antibody, Ascc2 antibody
    背景
    ASCC2 (activating signal cointegrator 1 complex subunit 2), also known as ASC1P100, is a 757 amino acid protein that is ubiquitously expressed and contains one CUE domain.The gene encoding ASCC2 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
    分子量
    86 kDa
    NCBI登录号
    NP_115580
    UniProt
    Q9H1I8
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