电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

GTF2I 抗体 (C-Term)

This anti-GTF2I antibody (ABIN7448970) is a Rabbit Polyclonal antibody detecting GTF2I in IHC, IF (p). Suitable for Human, Mouse.
产品编号 ABIN7448970
发货至: 中国

Quick Overview for GTF2I 抗体 (C-Term) (ABIN7448970)

抗原

See all GTF2I 抗体
GTF2I (General Transcription Factor III (GTF2I))

适用

  • 52
  • 24
  • 19
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
人, 小鼠

宿主

  • 48
  • 4

克隆类型

  • 48
  • 4
多克隆

标记

  • 35
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GTF2I antibody is un-conjugated

应用范围

  • 41
  • 23
  • 15
  • 15
  • 8
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 8
    • 8
    • 7
    • 4
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    原理

    Rabbit anti-GTF2I/TFII-I IHC Antibody, Affinity Purified

    预测反应

    Rat,Orangutan,Monkey,Chimpanzee,White-tufted-ear marmoset,Crab-eating macaque,Little brown bat,Small-eared galago,Northern white-cheeked gibbon

    纯化方法

    Affinity Purified

    免疫原

    Between AA 950 and C-term

    亚型

    IgG
  • 应用备注

    IHC-IF: 1:50 - 1:500

    IHC: 1:100 - 1:500

    限制

    仅限研究用
  • 浓度

    100 μg/mL

    缓冲液

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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

    4 °C

    有效期

    12 months
  • 抗原

    GTF2I (General Transcription Factor III (GTF2I))

    别名

    GTF2I/TFII-I

    背景

    Background: GTF2I/TFII-I is a multi-functional transcription factor that interacts with the basal transcription machinery and links upstream cellular signals to responsive activator complexes that associate with the C-FOS promoter and other response elements. Haploinsufficiency of GTF2I/TFII-I results in Williams-Beuren syndrome (WBS), a rare developmental disorder characterized by musculo-skeletal and cardiac abnormalities.

    基因ID

    2969

    NCBI登录号

    NP_127492

    UniProt

    P78347
You are here:
Chat with us!