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SMCR7 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

SMCR7 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 ABIN2732246
发货至: 中国
  • 抗原 See all SMCR7 蛋白
    SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 3
    • 2
    • 1
    资源
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This SMCR7 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human SMCR7 (transcript variant 1) 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 SMCR7 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
    SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
    别名
    Smcr7 (SMCR7 产品)
    别名
    AI482195 Protein, Gm11 Protein, MID49 Protein, mid49 Protein, Smcr7 Protein, RGD1560728 Protein, SMCR7 Protein, im:7149098 Protein, smcr7 Protein, smcr7b Protein, zgc:152920 Protein, mitochondrial elongation factor 2 Protein, mitochondrial elongation factor 2 S homeolog Protein, Mief2 Protein, MIEF2 Protein, mief2.S Protein, mief2 Protein
    背景
    This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms.
    分子量
    49.1 kDa
    NCBI登录号
    NP_631901
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