TPGS2 anticorps
Aperçu rapide pour TPGS2 anticorps (ABIN7230614)
Antigène
Voir toutes TPGS2 (C18orf10) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
-
-
Fonction
- Rabbit Anti-PGS2 Polyclonal Antibody
-
Specificité
- The antibody detects endogenous levels of PGS2 protein
-
Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-
Immunogène
- Synthesized peptide derived from part region of human PGS2 protein
-
Isotype
- IgG
-
-
-
-
Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000
-
Restrictions
- For Research Use only
-
-
-
Format
- Liquid
-
Concentration
- 1 mg/mL
-
Buffer
- PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA
-
Agent conservateur
- ProClin
-
Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Stock
- -20 °C
-
Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
-
Date de péremption
- 12 months
-
-
- TPGS2 (C18orf10) (Chromosome 18 Open Reading Frame 10 (C18orf10))
-
Autre désignation
- PGS2
-
Sujet
- Decorin, Bone proteoglycan II, PG-S2, PG40DCN encodes a member of the small leucine-rich proteoglycan family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. Decorin plays a role in collagen fibril assembly. Binding of this protein to multiple cell surface receptors mediates its role in tumor suppression, including a stimulatory effect on autophagy and inflammation and an inhibitory effect on angiogenesis and tumorigenesis. This gene and the related gene biglycan are thought to be the result of a gene duplication. Mutations in this gene are associated with congenital stromal corneal dystrophy in human patients.
-
Poids moléculaire
- 39kD
-
ID gène
- 1634
-
UniProt
- P07585
Antigène
-