ADAMTS13 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2714385

Détail du produit

Antigène: ADAMTS13 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette ADAMTS13 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human ADAMTS13 (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: ADAMTS13 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13))

Autre désignation: Adamts13 (ADAMTS13 Produits)

Synonymes: ADAMTS13 Protein, ADAM-TS13 Protein, ADAMTS-13 Protein, C9orf8 Protein, VWFCP Protein, vWF-CP Protein, Gm710 Protein, ADAM metallopeptidase with thrombospondin type 1 motif 13 Protein, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13 Protein, ADAM metallopeptidase with thrombospondin type 1 motif, 13 Protein, ADAMTS13 Protein, Adamts13 Protein, adamts13 Protein

Sujet: This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 149.9 kDa

NCBI Accession: NP_620594