ROR2 Antikörper (AA 59-155)

Produktnummer ABIN2683012

Produktdetails anti-ROR2 Antikörper

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

Bindungsspezifität: AA 59-155

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser ROR2 Antikörper ist unkonjugiert

Applikation: ELISA, Flow Cytometry (FACS)

Verwendungszweck: ROR2 Antibody

Aufreinigung: Purified antibody

Immunogen: Purified recombinant fragment of human ROR2 (AA: 59-155) expressed in E. Coli.

Klon: 6F2D10

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise:

ELISA: 1/10000

FCM: 1/200 - 1/400

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified antibody in PBS with 0.05 % sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C short term. Aliquot and store at -20°C long term. 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:

Description: 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.

Aliases: BDB, BDB1, NTRKR2

Molekulargewicht: 104.8kDa

Gen-ID: 4920

HGNC: 4920

UniProt: Q01974

Pathways: RTK Signalweg, WNT Signalweg