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PEX1 抗体 (AA 256-1266)

This anti-PEX1 antibody is a 兔 多克隆 antibody detecting PEX1 in WB, ELISA, IHC, IF 和 FACS. Suitable for 人.
产品编号 ABIN7825671
发货至: 中国

Quick Overview for PEX1 抗体 (AA 256-1266) (ABIN7825671)

抗原

See all PEX1 抗体
PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

适用

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  • 9
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宿主

  • 27
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  • 1

克隆类型

  • 30
多克隆

标记

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  • 1
This PEX1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)
  • 抗原表位

    • 8
    • 5
    • 2
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    • 1
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    AA 256-1266

    原理

    Anti-PEX1 Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins

    产品特性

    Anti-PEX1 Antibody catalog # A03025-1. Tested in WB, IHC, IF, Flow Cytometry, ELISA applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human PEX1 recombinant protein (Position: Q256-R1266). Human PEX1 shares 83.4% amino acid (aa) sequence identity with mouse PEX1.

    亚型

    IgG
  • 应用备注

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry, 2-5 μg/mL, Human
    Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • 抗原

    PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

    别名

    PEX1

    背景

    This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene.

    分子量

    143 kDa

    基因ID

    5189

    UniProt

    O43933
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