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FIBIN 抗体 (AA 101-200) (FITC)

This anti-FIBIN antibody is a 兔 多克隆 antibody detecting FIBIN in WB, IF (cc) 和 IF (p). Suitable for 小鼠.
产品编号 ABIN6986828
发货至: 中国

Quick Overview for FIBIN 抗体 (AA 101-200) (FITC) (ABIN6986828)

抗原

See all FIBIN 抗体
FIBIN (Fin Bud Initiation Factor Homolog (FIBIN))

适用

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小鼠

宿主

  • 20
  • 1

克隆类型

  • 21
多克隆

标记

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This FIBIN antibody is conjugated to FITC

应用范围

  • 17
  • 12
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  • 7
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 5
    • 1
    • 1
    AA 101-200

    交叉反应

    小鼠

    预测反应

    Human,Rat,Cow,Sheep,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human FIBIN

    亚型

    IgG
  • 应用备注

    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

    FIBIN (Fin Bud Initiation Factor Homolog (FIBIN))

    别名

    FIBIN

    背景

    Synonyms: Fin bud initiation factor homolog, FIBIN, PSEC0235

    Background: FIBIN (Fin bud initiation factor homolog) is a 211 amino acid protein involved in fin initiation in zebrafish. The human homolog is encoded by a gene that maps to chromosome 11, which makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

    基因ID

    387758

    UniProt

    Q8TAL6
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