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PRDM16 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

PRDM16 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 ABIN2729560
发货至: 中国
  • 抗原 See all PRDM16 蛋白
    PRDM16 (PR Domain Containing 16 (PRDM16))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 2
    • 1
    • 1
    资源
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This PRDM16 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human PRDM16 (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 PRDM16 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
    PRDM16 (PR Domain Containing 16 (PRDM16))
    别名
    Prdm16 (PRDM16 产品)
    别名
    PRDM16 Protein, wu:fc09g08 Protein, MEL1 Protein, PFM13 Protein, 5730557K01Rik Protein, C130091E20 Protein, csp1 Protein, mKIAA1675 Protein, mel1 Protein, PR/SET domain 16 Protein, PR domain containing 16 Protein, PRDM16 Protein, prdm16 Protein, Prdm16 Protein
    背景
    The reciprocal translocation t(13)(p36q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported.
    分子量
    140.1 kDa
    NCBI登录号
    NP_071397
    途径
    Stem Cell Maintenance, Brown Fat Cell Differentiation
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