TJP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2733788

Détail du produit

Antigène: TJP2 (Tight Junction Protein 2 (Zona Occludens 2) (TJP2))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette TJP2 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human TJP2 (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: TJP2 (Tight Junction Protein 2 (Zona Occludens 2) (TJP2))

Autre désignation: Tjp2 (TJP2 Produits)

Synonymes: C9DUPq21.11 Protein, DFNA51 Protein, DUP9q21.11 Protein, X104 Protein, ZO2 Protein, ZO-2 Protein, zo2 Protein, tjp2 Protein, x104 Protein, zo-2 Protein, wu:fb62b09 Protein, zgc:92094 Protein, tight junction protein 2 Protein, tight junction protein 2 L homeolog Protein, tight junction protein 2b (zona occludens 2) Protein, TJP2 Protein, Tjp2 Protein, tjp2.L Protein, tjp2b Protein

Sujet: This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene.

Poids moléculaire: 133.8 kDa

NCBI Accession: NP_004808