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MSH5 Protein (Transcript Variant 4) (Myc-DYKDDDDK Tag)

MSH5 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2726437
发货至: 中国
  • 抗原 See all MSH5 蛋白
    MSH5 (MutS Homolog 5 (MSH5))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 4
    宿主
    • 3
    • 1
    资源
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This MSH5 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human MSH5 (transcript variant 4) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MSH5 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    MSH5 (MutS Homolog 5 (MSH5))
    别名
    Msh5 (MSH5 产品)
    别名
    MSH5 Protein, G7 Protein, MUTSH5 Protein, NG23 Protein, Mut5 Protein, mutS homolog 5 Protein, mutS protein homolog 5 Protein, MSH (MutS Homolog) family Protein, MSH5 Protein, msh5 Protein, LOC100635155 Protein, Msh5 Protein, msh-5 Protein
    背景
    This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene.
    分子量
    92.7 kDa
    NCBI登录号
    NP_751898
    途径
    M Phase
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