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AMPD1 Protein (Myc-DYKDDDDK Tag)

AMPD1 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 ABIN2714666
发货至: 中国
  • 抗原 See all AMPD1 蛋白
    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
    蛋白类型
    Recombinant
    宿主
    • 2
    • 1
    • 1
    资源
    • 1
    • 1
    • 1
    • 1
    HEK-293 Cells
    标记
    This AMPD1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human AMP deaminase 1 / AMPD1 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 AMPD1 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
    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
    别名
    Amp Deaminase 1,ampd1 (AMPD1 产品)
    别名
    ampd1 Protein, MAD Protein, MADA Protein, AI553520 Protein, Ampd-1 Protein, Ampd01 Protein, RATAMPD01 Protein, zgc:77905 Protein, adenosine monophosphate deaminase 1 Protein, N-acetyl-anhydromuranmyl-L-alanine amidase Protein, N-acetylmuramoyl-L-alanine amidase Protein, Negative regulator of beta-lactamase expression Protein, adenosine monophosphate deaminase 1 (isoform M) Protein, AMPD1 Protein, ampD1 Protein, ampd1 Protein, Ampd1 Protein
    背景
    Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010].
    分子量
    90 kDa
    NCBI登录号
    NP_000027
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