C2 Mouse Monoclonal Antibody [Clone ID: LBI1A7]
Product Specifications
Background
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]
Synonyms
ARMD14; CO2
Gene Name
Homo sapiens complement C2 (C2), transcript variant 1, mRNA.
Gene ID
717
UniProt
P06681
Conjugation
Unconjugated
Related Pathways
Complement and coagulation cascades, Systemic lupus erythematosus
Field of Research
Complement and coagulation cascades, Systemic lupus erythematosus
Dilution
WB 1:500, IHC 1:150
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
Druggable Genome, Protease, Secreted Protein
Storage Conditions
Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
C2
Overview
Carrier-free (BSA/glycerol-free) C2 mouse monoclonal antibody, clone LBI1A7
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=717
Uniprot URL
https://www.uniprot.org/uniprot/P06681
Curated Selection
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