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PEX12 抗体 (AA 290-359)

This 兔 多克隆 anti-PEX12 antibody specifically detects PEX12 in WB. The antibody is reactive with 人 samples.
产品编号 ABIN7269246
发货至: 中国
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Quick Overview for PEX12 抗体 (AA 290-359) (ABIN7269246)

抗原

See all PEX12 抗体
PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

适用

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宿主

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克隆类型

  • 17
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多克隆

标记

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This PEX12 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    AA 290-359

    原理

    PEX12 Rabbit pAb

    序列

    YNSDSPLLPK MKTVCPLCRK TRVNDTVLAT SGYVFCYRCV FHYVRSHQAC PITGYPTEVQ HLIKLYSPEN

    交叉反应

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 290-359 of human PEX12 (NP_000277.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

    别名

    PEX12

    背景

    This gene belongs to the peroxin-12 family. 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. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 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 are a cause of Zellweger syndrome (ZWS).,PEX12,PAF-3,PBD3A,Signal Transduction,PEX12

    分子量

    40kDa

    基因ID

    5193

    UniProt

    O00623
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