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EIF4H 抗体 (AA 1-248)

This anti-EIF4H antibody is a 兔 多克隆 antibody detecting EIF4H in WB, ELISA, IF, ICC 和 FACS. Suitable for 人 和 猴.
产品编号 ABIN7825370
发货至: 中国

Quick Overview for EIF4H 抗体 (AA 1-248) (ABIN7825370)

抗原

See all EIF4H 抗体
EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))

适用

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人, 猴

宿主

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克隆类型

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多克隆

标记

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This EIF4H antibody is un-conjugated

应用范围

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

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    AA 1-248

    原理

    Anti-EIF4H Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins

    产品特性

    Anti-EIF4H Antibody catalog # A05539-1. Tested in WB, ICC/IF, Flow Cytometry, ELISA applications. This antibody reacts with Human, Monkey. 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 EIF4H recombinant protein (Position: M1-E248). Human EIF4Hshares 98.8% and 98% amino acid (aa) sequence identity with mouse and rat EIF4H, respectively.

    亚型

    IgG
  • 应用备注

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

    EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))

    别名

    EIF4H

    背景

    This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.

    分子量

    25 kDa

    基因ID

    7458

    UniProt

    Q15056

    途径

    SARS-CoV-2 Protein Interactome
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