Skip to content

Datenblatt ansehen

open_in_new
  1. Alles ansehen
  2. Polyclonal

GTX54941

ADAMTS2 antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX54941
Zusätzliche Namen:
ADAM metallopeptidase with thrombospondin type 1 motif 2 , ADAM-TS2 , ADAMTS-2 , ADAMTS-3 , EDSDERMS , NPI , PC I-NP , PCI-NP , PCINP , PCPNI , PNPI
Anwendung:
WB
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Buffer:
0.42% Potassium Phosphate, 0.87% NaCl, 30% Glycerol, 0.01% Sodium azide.
Immunogen:
KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of ADAMTS2. The exact sequence is proprietary.
Uniprot:
O95450
Synonyme:
A disintegrin and metalloproteinase with thrombospondin motifs 2;a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2;ADAM-TS2;ADAMTS-2;ADAMTS-3;EDSDERMS;NPI;PC I-NP;PCI-NP;PCINP;PCPNI;PNPI;procollagen I N-proteinase;procollagen I/II amino propeptide-processing enzyme;procollagen N-endopeptidase
Weitere Details:
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. [provided by RefSeq, Feb 2016]
Versandbedingungen:
Blue Ice