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Peroxidasin 抗体 (AA 900-1054)

This 兔 多克隆 anti-Peroxidasin antibody specifically detects Peroxidasin in WB, IHC 和 ELISA. The antibody is reactive with 人 samples.
产品编号 ABIN7825669
发货至: 中国
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Quick Overview for Peroxidasin 抗体 (AA 900-1054) (ABIN7825669)

抗原

See all Peroxidasin (PXDN) 抗体
Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

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 Peroxidasin antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC), ELISA
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    AA 900-1054

    原理

    Anti-PXDN Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins

    产品特性

    Anti-PXDN Antibody catalog # A06456-1. Tested in WB, IHC, 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 PXDN recombinant protein (Position: R900-D1054). Human PXDN shares 94.8% amino acid (aa) sequence identity with mouse PXDN.

    亚型

    IgG
  • 应用备注

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry, 2-5 μg/mL, 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

    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

    别名

    PXDN

    背景

    This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.

    分子量

    165 kDa

    基因ID

    7837

    UniProt

    Q92626
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