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MUTYH 抗体 (AA 1801-1939) (AbBy Fluor® 750)

This anti-MUTYH antibody is a 兔 多克隆 antibody detecting MUTYH in FACS, IF (cc) 和 IF (p). Suitable for 人 和 小鼠.
产品编号 ABIN5007192
发货至: 中国

Quick Overview for MUTYH 抗体 (AA 1801-1939) (AbBy Fluor® 750) (ABIN5007192)

抗原

See all MUTYH 抗体
MUTYH (MutY Homolog (E. Coli) (MUTYH))

适用

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人, 小鼠

宿主

  • 48
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克隆类型

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多克隆

标记

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This MUTYH antibody is conjugated to AbBy Fluor® 750

应用范围

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Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 15
    • 5
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    AA 1801-1939

    交叉反应

    人, 小鼠

    预测反应

    Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human MYH 6

    亚型

    IgG
  • 应用备注

    FCM 1:20-100
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    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.

    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

    MUTYH (MutY Homolog (E. Coli) (MUTYH))

    别名

    MYH

    背景

    Synonyms: Alpha MHC, ASD3, CMD1S, CMH1, MGC138376, MGC138378, MPD1, MYH 6, MYH 7, MYH6, MYH7, MYHC A, MYHC, MYHC B, MyHC-alpha, MyHC-beta, MYHCA, MYHCB, Myosin heavy chain cardiac muscle alpha isoform, Myosin heavy chain cardiac muscle beta isoform, Myosin heavy polypeptide 7 cardiac muscle beta, MYH6_HUMAN, MYH7_HUMAN.

    Background: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.

    基因ID

    4625

    途径

    DNA Damage Repair
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