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PEX7 抗体 (AA 180-260)

This 兔 多克隆 anti-PEX7 antibody specifically detects PEX7 in WB, ELISA 和 IHC (p). The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7223122
发货至: 中国
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Quick Overview for PEX7 抗体 (AA 180-260) (ABIN7223122)

抗原

See all PEX7 抗体
PEX7 (Peroxisomal Biogenesis Factor 7 (PEX7))

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

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  • 7
多克隆

标记

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This PEX7 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 15
    • 6
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    AA 180-260

    原理

    Peroxin 7 Polyclonal Antibody

    特异性

    Peroxin 7 Polyclonal Antibody detects endogenous levels of Peroxin 7 protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen

    免疫原

    Synthesized peptide derived from the Internal region of human Peroxin 7 at AA range: 180-260

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS containing 50 % Glycerol, 0.5 % BSA and 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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    PEX7 (Peroxisomal Biogenesis Factor 7 (PEX7))

    别名

    Peroxin 7

    背景

    Rabbit Anti-Peroxin 7 Polyclonal Antibody,PEX7, PTS2R, Peroxisomal targeting signal 2 receptor, PTS2 receptor, Peroxin-7,PEX7 (peroxisomal biogenesis factor 7) encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in PEX7 cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular 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 have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD).,Peroxisomal targeting signal 2 receptor

    分子量

    observerd band 40kDa

    基因ID

    5191

    UniProt

    O00628

    途径

    Monocarboxylic Acid Catabolic Process
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