ATP7B Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2715066

Détail du produit

Antigène: ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette ATP7B protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human ATP7B (transcript variant 1) 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: ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))

Autre désignation: Atp7b (ATP7B Produits)

Synonymes: PWD Protein, WC1 Protein, WD Protein, WND Protein, Atp7a Protein, tx Protein, Hts Protein, PINA Protein, Wd Protein, ATP7B Protein, ATPase copper transporting beta Protein, ATPase, Cu++ transporting, beta polypeptide Protein, ATPase, Cu++ transporting, beta polypeptide (Wilson disease) Protein, copper-transporting ATPase 2 Protein, ATP7B Protein, Atp7b Protein, atp7b Protein, LOC592143 Protein

Sujet: This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).

Poids moléculaire: 157.1 kDa

NCBI Accession: NP_000044

Pathways: Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process