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HGD Protein (Myc-DYKDDDDK Tag)

HGD 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 ABIN2722962
发货至: 中国
  • 抗原 See all HGD 蛋白
    HGD (Homogentisate 1,2-Dioxygenase (HGD))
    蛋白类型
    Recombinant
    宿主
    • 8
    • 3
    • 1
    资源
    • 6
    • 3
    • 2
    • 1
    HEK-293 Cells
    标记
    This HGD protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Homogentisicase / HGD 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 HGD 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
    HGD (Homogentisate 1,2-Dioxygenase (HGD))
    别名
    Homogentisicase,hgd (HGD 产品)
    别名
    CG4779 Protein, Dmel\\CG4779 Protein, PSPTO3551 Protein, DDBDRAFT_0185702 Protein, DDBDRAFT_0191461 Protein, DDB_0185702 Protein, DDB_0191461 Protein, Hgo Protein, aku Protein, hgo Protein, AKU Protein, HGO Protein, homogentisate 1,2-dioxygenase Protein, Homogentisate 1,2-dioxygenase Protein, homogentisate 1, 2-dioxygenase Protein, homogentisate 1,2-dioxygenase L homeolog Protein, hgo Protein, HGD Protein, hmgA Protein, Shewana3_2481 Protein, hgd Protein, BC1002_0545 Protein, BC1003_0502 Protein, BC1001_0489 Protein, Sinme_2995 Protein, Sphch_0441 Protein, Hgd Protein, hgd.L Protein
    背景
    This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010].
    分子量
    49.8 kDa
    NCBI登录号
    NP_000178
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