ROR2 Antikörper
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- Target Alle ROR2 Antikörper anzeigen
- ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
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Reaktivität
- Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser ROR2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human ROR2 (NP_004551.2).
- Isotyp
- IgG
- Top Product
- Discover our top product ROR2 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- 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.
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- 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
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Observed_MW: 145 kDa
Calculated_MW: 104 kDa
- Gen-ID
- 4920
- UniProt
- Q01974
- Pathways
- RTK Signalweg, WNT Signalweg
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