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PMS2CL/PMS2 抗体 (N-Term)

PMS2 适用: 人 IP, WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7468755
发货至: 中国
  • 抗原 See all PMS2CL/PMS2 (PMS2) products
    PMS2CL/PMS2 (PMS2) (PMS1 Homolog 2, Mismatch Repair System Component (PMS2))
    抗原表位
    N-Term
    适用
    宿主
    • 1
    克隆类型
    • 1
    多克隆
    标记
    • 1
    This PMS2CL/PMS2 antibody is un-conjugated
    应用范围
    Immunoprecipitation (IP), Western Blotting (WB)
    交叉反应
    纯化方法
    Purified by antigen-affinity chromatography.
    免疫原
    Recombinant protein encompassing a sequence within the N-terminus region of human PMS2. The exact sequence is proprietary.
    亚型
    IgG
  • 应用备注
    WB: 1:500-1:10000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    说明

    Positive Control: human PMS2-transfected 293T cells , A431 , HeLa , HepG2 Validation: Overexpression

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300
    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
    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原
    PMS2CL/PMS2 (PMS2) (PMS1 Homolog 2, Mismatch Repair System Component (PMS2))
    别名
    PMS1 homolog 2, mismatch repair system component (PMS2 产品)
    别名
    HNPCC4 antibody, PMS2CL antibody, PMSL2 antibody, PMS1 homolog 2, mismatch repair system component antibody, PMS2 antibody
    背景

    Synonyms: PMS1 homolog 2, mismatch repair system component , HNPCC4 , MLH4 , PMS2CL , PMSL2

    Background: This gene is one of the PMS2 gene family members found in clusters on chromosome 7. The product of this gene is involved in DNA mismatch repair. It forms a heterodimer with MLH1 and this complex interacts with other complexes bound to mismatched bases. Mutations in this gene are associated with hereditary nonpolyposis colorectal cancer, Turcot syndrome, and are a cause of supratentorial primitive neuroectodermal tumors. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq]

    分子量
    96 kDa
    基因ID
    5395
    UniProt
    P54278
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