ROR2 Antikörper

Produktnummer ABIN7009688

Produktdetails anti-ROR2 Antikörper

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

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ROR2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ROR2

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

Andere Bezeichnung: ROR2 (ROR2 Produkte)

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

Hintergrund: 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.

Molekulargewicht:

Observed_MW: 145 kDa

Calculated_MW: 104 kDa

Gen-ID: 4920

UniProt: Q01974

Pathways: RTK Signalweg, WNT Signalweg