製品の概要

製品の詳細

  • 由来Recombinant
  • 由来Wheat germ
  • アミノ酸配列
    • アクセッション番号P55316
    • 生物種Human
    • 配列SPFLSLHHPRASSTLSYNGTTSAYPSHPMPYSSVLTQNSLGNNHSFSTAN GLSVDRLVNGE
    • 分子量32 kDa including tags
    • 領域164 to 224

特性

Our Abpromise guarantee covers the use of ab114230 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • アプリケーション

    ELISA

    SDS-PAGE

    Western blot

  • 製品の状態Liquid
  • 備考Protein concentration is above or equal to 0.05 mg/ml
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

関連情報

  • 別名
    • BF-1
    • BF-2
    • BF1
    • BF2
    • Brain factor 1
    • Brain factor 2
    • FHKL
    • FKH2
    • FKHL1
    • FKHL2
    • FKHL3
    • FKHL4
    • Forkhead box protein G1
    • Forkhead box protein G1A
    • Forkhead box protein G1B
    • Forkhead box protein G1C
    • Forkhead like 1
    • Forkhead like 2
    • Forkhead like 3
    • Forkhead like 4
    • Forkhead-related protein FKHL1
    • Forkhead-related protein FKHL2
    • Forkhead-related protein FKHL3
    • FOXG1
    • FOXG1_HUMAN
    • FOXG1A
    • FOXG1B
    • FOXG1C
    • HBF 1
    • HBF G2
    • hBF-2
    • HBF2
    • HFK1
    • HFK2
    • HFK3
    • KHL2
    • Oncogene QIN
    • QIN
    see all
  • 機能Transcription repression factor which plays an important role in the establishment of the regional subdivision of the developing brain and in the development of the telencephalon.
  • 組織特異性Expression is restricted to the neurons of the developing telencephalon.
  • 関連疾患Defects in FOXG1 are the cause of congenital variant of Rett syndrome (RTTCV) [MIM:613454]. RTTCV is a severe neurodevelopmental disorder with features of classic Rett syndrome but earlier onset in the first months of life. Clinical features include progressive microcephaly, hypotonia, irresponsiveness and irritability in the neonatal period, mental retardation, psychomotor regression and stereotypical movements.
  • 配列類似性Contains 1 fork-head DNA-binding domain.
  • 細胞内局在Nucleus.
  • Information by UniProt

Recombinant Human FOXG1 protein 画像

  • 12.5% SDS-PAGE showing ab114230 at approximately 32.24kDa stained with Coomassie Blue.

Recombinant Human FOXG1 protein (ab114230) 使用論文

ab114230 has not yet been referenced specifically in any publications.

Product Wall

There are currently no Abreviews or Questions for ab114230.
Please use the links above to contact us or submit feedback about this product.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"