Imagine indisponibilăAnti-ROR2 Antibody [ROR2/1912]
Pe scurt
Anti-ROR2 Antibody [ROR2/1912] este un anticorp monoclonal de șoarece împotriva țintei ROR2, cu reactivitate declarată pentru Human. Este validat pentru IHC-P, are izotipul IgG și se livrează neconjugat. Se livrează în mărimea 100µg, la prețul de 3.826,63 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse monoclonal [ROR2/1912] antibody to ROR2.
Specificații
- Brand
- Antibodies
- Mărime
- 100µg
- Țintă
- ROR2
- Applications
- IHC-P
- Reactivity
- Human
- Conjugate
- Unconjugated
- Host
- Mouse
- Clonality
- Monoclonal
- Product form
- Liquid
- Concentration
- 200 µg/ml
- Purification
- Protein A/G chromatography.
- Isotype
- IgG
- Recommended dilutions
- IHC-P: 1-2 µg/ml
- Molecular weight
- 120 kDa
- Clonă
- ROR2/1912
- Imunogen
- Human cultured keratinocytes.
- Specificitate
- ROR2 (receptor tyrosine kinase-like orphan receptor 2), also known as neurotrophic tyrosine kinase receptor-related 2 (NTRKR2), is a single pass transmembrane tyrosine-protein kinase receptor. It contains a cytoplasmic tyrosine kinase domain, distally located serine-threonine-rich domains, an extracellular immunoglobulin-like domain, a cysteine-rich domain and a kringle domain. ROR2 is important for skeletal and endocrine development and is required for cartilage and growth plate development. It promotes the differentiation of osteoblasts and plays an important role in the early formation of chondrocytes. ROR2 sequesters and associates with Dlxin-1 affecting the transcriptional function of Msx-2. ROR2 also interacts with canoncial Wnt-1 and Wnt-3, regulating their signaling pathways. Defects in ROR2 can result in the autosomal dominant skeletal disorder, brachydactyly type B1, or the autosomal recessive skeletal disorder, Robinow syndrome.
Documentație
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