FOXI1 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

N° du produit ABIN2721357

Détail du produit

Antigène: FOXI1 (Forkhead Box I1 (FOXI1))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 2

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette FOXI1 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human FOXI1 / FKHL10 (transcript variant 2) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

Antigène: FOXI1 (Forkhead Box I1 (FOXI1))

Autre désignation: Foxi1,fkhl10 (FOXI1 Produits)

Synonymes: FKH10 Protein, FKHL10 Protein, FREAC-6 Protein, FREAC6 Protein, HFH-3 Protein, HFH3 Protein, 5830401E05Rik Protein, Fkh10 Protein, Hfh3 Protein, cb724 Protein, foo Protein, Xfoxi1a Protein, ema Protein, foxi1a Protein, foxi1e Protein, xema Protein, xfoxi1 Protein, FoxI1e Protein, Xema Protein, fkhl10 Protein, freac6 Protein, hfh3 Protein, FOXI1 Protein, forkhead box I1 Protein, forkhead box i1 Protein, forkhead box I1 L homeolog Protein, forkhead box protein I1 Protein, FOXI1 Protein, Foxi1 Protein, foxi1 Protein, foxi1.L Protein, CC1G_14832 Protein

Sujet: This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4.

Poids moléculaire: 30.6 kDa

NCBI Accession: NP_658982