ROR2 anticorps (AA 450-530)
Aperçu rapide pour ROR2 anticorps (AA 450-530) (ABIN7222848)
Antigène
Voir toutes ROR2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
-
-
Épitope
- AA 450-530
-
Fonction
- ROR2 Polyclonal Antibody
-
Specificité
- ROR2 Polyclonal Antibody detects endogenous levels of ROR2 protein.
-
Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
-
Immunogène
- Synthesized peptide derived from the Internal region of human ROR2 at AA range: 450-530
-
Isotype
- IgG
-
-
-
-
Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000). Not yet tested in other applications.
-
Commentaires
-
Primary Antibody
-
Restrictions
- For Research Use only
-
-
-
Format
- Liquid
-
Concentration
- 1 mg/mL
-
Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
-
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
- 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.
-
-
- ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
-
Autre désignation
- ROR2
-
Sujet
- Rabbit Anti-ROR2 Polyclonal Antibody,ROR2, NTRKR2, Tyrosine-protein kinase transmembrane receptor ROR2, Neurotrophic tyrosine kinase, receptor-related 2,The protein encoded by ROR2 is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in ROR2 can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.,Tyrosine-protein kinase transmembrane receptor ROR2
-
Poids moléculaire
- observerd band 110kDa
-
ID gène
- 4920
-
UniProt
- Q01974
-
Pathways
- Signalisation RTK, Signalisation WNT
Antigène
-