Adamts2 anticorps

N° du produit ABIN7255235

Détail du produit anti-Adamts2 anticorps

Antigène: Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Adamts2 est non-conjugé

Application: Western Blotting (WB)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of mouse ADAMTS2

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur Adamts2

Antigène: Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))

Autre désignation: ADAMTS2 (Adamts2 Produits)

Synonymes: anticorps ADAM-TS2, anticorps ADAMTS-2, anticorps ADAMTS-3, anticorps PCINP, anticorps hPCPNI, anticorps mKIAA4060, anticorps pNPI, anticorps NPI, anticorps PC I-NP, anticorps PCI-NP, anticorps PCPNI, anticorps PNPI, anticorps RGD1565950, anticorps a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2, anticorps ADAM metallopeptidase with thrombospondin type 1 motif 2, anticorps ADAM metallopeptidase with thrombospondin type 1 motif, 2, anticorps Adamts2, anticorps ADAMTS2

Sujet: This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.

Poids moléculaire:

Observed_MW: 120 kDa

Calculated_MW: 61 kDa/134 kDa

ID gène: 216725

UniProt: Q8C9W3