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FAM111A 抗体 (AA 264-314)

This 兔 多克隆 antibody specifically detects FAM111A in WB. It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN8121365
发货至: 中国
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Quick Overview for FAM111A 抗体 (AA 264-314) (ABIN8121365)

抗原

FAM111A (Family with Sequence Similarity 111, Member A (FAM111A))

适用

人, 小鼠

宿主

  • 7
  • 1
兔

克隆类型

  • 7
  • 1
多克隆

标记

  • 4
  • 2
  • 1
  • 1
This FAM111A antibody is un-conjugated

应用范围

  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)
  • 抗原表位

    • 5
    • 1
    • 1
    AA 264-314

    原理

    F111A Antibody

    特异性

    This antibody detects endogenous levels of F111A at Human/Mouse

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    Synthesized peptide derived from human F111A AA range: 264-314

    亚型

    IgG
  • 应用备注

    WB 1:500-2000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: 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/1 year

    有效期

    12 months
  • 抗原

    FAM111A (Family with Sequence Similarity 111, Member A (FAM111A))

    别名

    F111A

    背景

    Background: The protein encoded by this gene is cell-cycle regulated, and has nuclear localization. The C-terminal half of the protein shares homology with trypsin-like peptidases and it contains a PCNA-interacting peptide (PIP) box, that is necessary for its co-localization with proliferating cell nuclear antigen (PCNA). Reduced expression of this gene resulted in DNA replication defects, consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication. Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS, also known as Gracile Bone Dysplasia), both characterized by short stature, hypoparathyroidism, bone development abnormalities, and hypocalcemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015],

    Gene Name: FAM111A KIAA1895

    Protein Name: F111A

    基因ID

    63901

    UniProt

    Q96PZ2
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