Mouse Anti-COL13A1 Recombinant Antibody (CBXC-1257) (V2LY-1206-LY595)
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Basic Information
| Application | Note |
| IHC | 8-25 µg/ml |
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Cell differentiation Source: UniProtKB-KW
Cell-matrix adhesion Source: UniProtKB
Collagen catabolic process Source: Reactome
Collagen fibril organization Source: GO_Central
Endochondral ossification Source: UniProtKB
Extracellular matrix organization Source: GO_Central
Morphogenesis of a branching structure Source: UniProtKB
Notochord development Source: GO_Central
Skeletal system development Source: GO_Central
A form of congenital myasthenic syndrome, a group of disorders characterized by failure of neuromuscular transmission, including pre-synaptic, synaptic, and post-synaptic disorders that are not of autoimmune origin. Clinical features are easy fatigability and muscle weakness affecting the axial and limb muscles (with hypotonia in early-onset forms), the ocular muscles (leading to ptosis and ophthalmoplegia), and the facial and bulbar musculature (affecting sucking and swallowing, and leading to dysphonia). The symptoms fluctuate and worsen with physical effort.
Helical: 45-61
Extracellular: 62-717
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols
Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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