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PHF8 抗体 (AA 108-946)

This anti-PHF8 antibody is a 兔 多克隆 antibody detecting PHF8 in WB, ICC, FACS, IF 和 ELISA. Suitable for 人.
产品编号 ABIN7825675
发货至: 中国

Quick Overview for PHF8 抗体 (AA 108-946) (ABIN7825675)

抗原

See all PHF8 抗体
PHF8 (PHD Finger Protein 8 (PHF8))

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 PHF8 antibody is un-conjugated

应用范围

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

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    AA 108-946

    原理

    Anti-PHF8 Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins

    产品特性

    Anti-PHF8 Antibody catalog # A03288-2. Tested in WB, ICC/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 PHF8 recombinant protein (Position: H108-D946). Human PHF8 shares 94.6% amino acid (aa) sequence identity with mouse PHF8.

    亚型

    IgG
  • 应用备注

    Western blot, 0.25-0.5 μg/mL, Human
    Immunocytochemistry/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

    PHF8 (PHD Finger Protein 8 (PHF8))

    别名

    PHF8

    背景

    The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.

    分子量

    140 kDa

    基因ID

    23133
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