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

PHYH 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 ABIN2728871
发货至: 中国
  • 抗原 See all PHYH 蛋白
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 3
    • 1
    • 1
    • 1
    资源
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This PHYH protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human PHYH / PAHX (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 PHYH 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
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    别名
    Phyh,pahx (PHYH 产品)
    别名
    zgc:110203 Protein, LN1 Protein, LNAP1 Protein, PAHX Protein, PHYH1 Protein, RD Protein, AI256161 Protein, AI265699 Protein, Lnap1 Protein, phytanoyl-CoA 2-hydroxylase Protein, phytanoyl-CoA hydroxylase-like Protein, phytanoyl-CoA hydroxylase Protein, PHYH Protein, LOC478001 Protein, phyh Protein, Phyh Protein
    背景
    This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
    分子量
    35.4 kDa
    NCBI登录号
    NP_006205
    途径
    Monocarboxylic Acid Catabolic Process
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