IRF6 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2723808

Détail du produit

Antigène: IRF6 (Interferon Regulatory Factor 6 (IRF6))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette IRF6 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human IRF6 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: IRF6 (Interferon Regulatory Factor 6 (IRF6))

Autre désignation: Irf6 (IRF6 Produits)

Synonymes: IRF6 Protein, lps Protein, pit Protein, pps Protein, vws Protein, ofc6 Protein, xIRF-6 Protein, DKFZp469E012 Protein, LPS Protein, OFC6 Protein, PIT Protein, PPS Protein, PPS1 Protein, VWS Protein, VWS1 Protein, zgc:63500 Protein, AI876454 Protein, E230028I05Rik Protein, mirf6 Protein, interferon regulatory factor 6 Protein, interferon regulatory factor 6 S homeolog Protein, IRF6 Protein, irf6 Protein, irf6.S Protein, Irf6 Protein

Sujet: This gene encodes a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. The encoded protein may be a transcriptional activator. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. Mutations in this gene are also associated with non-syndromic orofacial cleft type 6. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2011]

Poids moléculaire: 52.9 kDa

NCBI Accession: NP_006138