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IQCF1 抗体 (HRP)

This anti-IQCF1 antibody (ABIN1418272) is a Rabbit Polyclonal antibody detecting IQCF1 in WB, IHC (p). Suitable for Human.
产品编号 ABIN1418272
发货至: 中国

Quick Overview for IQCF1 抗体 (HRP) (ABIN1418272)

抗原

IQCF1 (IQ Motif Containing F1 (IQCF1))

适用

宿主

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克隆类型

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多克隆

标记

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This IQCF1 antibody is conjugated to HRP

应用范围

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human IQCF1

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    注意事项

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    IQCF1 (IQ Motif Containing F1 (IQCF1))

    别名

    IQCF1

    背景

    Synonyms: IQ domain-containing protein F1, IQ mot containing F1, Iqcf1, IQCF1_HUMAN, MGC39725.

    Background: IQCF1 is an 81 amino acid protein encoded by the IQCF1 gene, which maps to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

    基因ID

    132141
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