电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

Phenylalanine Hydroxylase Protein (Myc-DYKDDDDK Tag)

宿主: 化学剂 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2728159
发货至: 中国
  • 抗原 See all Phenylalanine Hydroxylase 蛋白
    Phenylalanine Hydroxylase
    蛋白类型
    Recombinant
    宿主
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    化学剂
    资源
    • 4
    • 3
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This Phenylalanine Hydroxylase protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human PAH 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 Phenylalanine Hydroxylase 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
    Phenylalanine Hydroxylase
    别名
    Pah (Phenylalanine Hydroxylase 产品)
    别名
    cb877 Protein, wu:fb02f10 Protein, zgc:65981 Protein, GB18494 Protein, PAH Protein, pku Protein, pku1 Protein, DDBDRAFT_0206188 Protein, DDBDRAFT_0231664 Protein, DDB_0206188 Protein, DDB_0231664 Protein, AW106920 Protein, PH Protein, PKU Protein, PKU1 Protein, phenylalanine-4-hydroxylase Protein, phenylalanine hydroxylase Protein, protein henna Protein, phenylalanine 4-monooxygenase Protein, pah Protein, LOC408622 Protein, PAH Protein, CpipJ_CPIJ002149 Protein, Pah Protein
    物质类
    Chemical
    背景
    PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.
    分子量
    51.7 kDa
    NCBI登录号
    NP_000268
You are here:
客服