ROR2 anticorps

N° du produit ABIN7009688

Détail du produit anti-ROR2 anticorps

Antigène: ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ROR2 est non-conjugé

Application: Western Blotting (WB)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human ROR2 (NP_004551.2).

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 ROR2

Antigène: ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

Autre désignation: ROR2 (ROR2 Produits)

Synonymes: anticorps BDB, anticorps BDB1, anticorps NTRKR2, anticorps Ntrkr2, anticorps mRor2, anticorps ROR2, anticorps bdb, anticorps bdb1, anticorps Xror2, anticorps ntrkr2, anticorps MGC97773, anticorps LOC100219935, anticorps ror2, anticorps xror2, anticorps receptor tyrosine kinase like orphan receptor 2, anticorps receptor tyrosine kinase-like orphan receptor 2, anticorps receptor tyrosine kinase like orphan receptor 2 L homeolog, anticorps ROR2, anticorps Ror2, anticorps ror2, anticorps ror2.L

Sujet: The protein encoded by this gene 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 this gene 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.

Poids moléculaire:

Observed_MW: 145 kDa

Calculated_MW: 104 kDa

ID gène: 4920

UniProt: Q01974

Pathways: Signalisation RTK, Signalisation WNT