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FRAS1 抗体 (AA 1101-1200) (HRP)

FRAS1 适用: 人 ELISA, IHC (fro), IHC (p) 宿主: 兔 Polyclonal HRP
产品编号 ABIN1711305
发货至: 中国
  • 抗原 See all FRAS1 抗体
    FRAS1 (Fraser Syndrome 1 (FRAS1))
    抗原表位
    • 14
    • 1
    AA 1101-1200
    适用
    宿主
    • 15
    克隆类型
    • 15
    多克隆
    标记
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FRAS1 antibody is conjugated to HRP
    应用范围
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    Human,Mouse,Rat
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human FRAS1
    亚型
    IgG
    Top Product
    Discover our top product FRAS1 Primary Antibody
  • 应用备注
    IHC-P 1:200-400
    IHC-F 1:100-500
    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
    FRAS1 (Fraser Syndrome 1 (FRAS1))
    别名
    FRAS1 (FRAS1 产品)
    别名
    E130113P14Rik antibody, bl antibody, mKIAA1500 antibody, Fraser extracellular matrix complex subunit 1 antibody, FRAS1 antibody, Fras1 antibody
    背景

    Synonyms: Extracellular matrix protein FRAS1, Fras 1, Fras1, FRAS1_HUMAN, Fraser syndrome 1.

    Background: This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009].

    基因ID
    80144
    UniProt
    Q86XX4
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