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PEX19 抗体 (AA 51-269) (Fluoro488)

This 兔 多克隆 antibody specifically detects PEX19 in FACS. It exhibits reactivity toward 人.
产品编号 ABIN8020763
发货至: 中国
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Quick Overview for PEX19 抗体 (AA 51-269) (Fluoro488) (ABIN8020763)

抗原

See all PEX19 抗体
PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

适用

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宿主

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克隆类型

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多克隆

标记

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This PEX19 antibody is conjugated to Fluoro488

应用范围

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Flow Cytometry (FACS)
  • 抗原表位

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    AA 51-269

    原理

    Anti-PEX19 Antibody Fluoro488 Conjugated

    预测反应

    Human PEX19 shares 91.8%,94.5% amino acid (aa) sequence identity with mouse,rat PEX19,respectively.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human PEX19 recombinant protein (Position: Q51-A269). Human PEX19 shares 91.8% and 94.5% amino acid (aa) sequence identity with mouse and rat PEX19, respectively.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

    别名

    PEX19

    背景

    Background: Peroxisomal biogenesis factor 19 is a protein that in humans is encoded by the PEX19 gene. 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.

    Gene Full Name: peroxisomal biogenesis factor 19

    基因ID

    5824

    UniProt

    P40855
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