CORA1 rabbit pAb
This gene encodes a member of the fibrillar collagen family, and plays a role during the calcification of cartilage and the transition of cartilage to bone. The encoded protein product is a preproprotein. It includes an N-terminal signal peptide, which is followed by an N-terminal propetide, mature peptide and a C-terminal propeptide. The N-terminal propeptide contains thrombospondin N-terminal-like and laminin G-like domains. The mature peptide is a major triple-helical region. The C-terminal propeptide, also known as COLFI domain, plays crucial roles in tissue growth and repair. Mutations in this gene cause Steel syndrome. Alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Sep 2014],
Product Specifications
Background
UniProt
Q8IZC6
Swiss Prot
Q8IZC6
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human protein . at AA range: 1551-1600
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Molecular Weight
204kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
204kD
Fragment
IgG
Subcellular Location
Secreted, extracellular space, extracellular matrix. Found on some small banded collagen fibrils and meshworks. .
Gene ID (Human)
85301
Available Sizes
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