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PEX19 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

PEX19 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 ABIN2728692
发货至: 中国
  • 抗原 See all PEX19 蛋白
    PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    资源
    • 5
    • 5
    • 1
    • 1
    • 1
    HEK-293 Cells
    标记
    This PEX19 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Peroxin 19 / PEX19 (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 PEX19 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
    PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))
    别名
    Peroxin 19,pex19 (PEX19 产品)
    别名
    BEST:GH03076 Protein, CG5325 Protein, DmelPex19 Protein, Dmel\\CG5325 Protein, D1S2223E Protein, HK33 Protein, PBD12A Protein, PMP1 Protein, PMPI Protein, PXF Protein, PXMP1 Protein, Pxf Protein, PxF Protein, Peroxin-19 Protein, Peroxin 19 Protein, Peroxisomal farnesylated protein Protein, peroxisomal biogenesis factor 19 Protein, Pex19 Protein, Bm1_19905 Protein, PEX19 Protein
    背景
    This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants.
    分子量
    32.6 kDa
    NCBI登录号
    NP_002848
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