C2 (NM_000063) Human Recombinant Protein
CAT#: TP762664
Purified recombinant protein of Human complement component 2 (C2), transcript variant 1, full length, with N-GST and C-His tag, expressed in E.coli, 50ug
Other products for "C2"
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding the region full length of C2
|
Tag | N-GST and C-HIS |
Predicted MW | 111.3 kDa |
Concentration | >50 ug/mL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50mM Tris, pH8.0, 8M Urea |
Storage | Store at -80°C after receiving vials. |
Stability | Stable for at least 1 year from receipt of products under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_000054 |
Locus ID | 717 |
UniProt ID | P06681, Q5JP69, Q53HP3 |
Cytogenetics | 6p21.33 |
Refseq Size | 2862 |
Refseq ORF | 2256 |
Synonyms | ARMD14; CO2 |
Summary | Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009] |
Protein Families | Druggable Genome, Protease, Secreted Protein |
Protein Pathways | Complement and coagulation cascades, Systemic lupus erythematosus |
Documents
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