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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]

Overview

Carrier-free (BSA/glycerol-free) C2 mouse monoclonal antibody, clone LBI1A7

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

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/?term=717

Uniprot URL

https://www.uniprot.org/uniprot/P06681

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