Complement C2 antibody

Catalog No. ABIN7227992

This anti-Complement C2 antibody is a Rabbit Polyclonal antibody detecting Complement C2 in WB and ELISA. Suitable for Human and Mouse.

Quick Overview for Complement C2 antibody (ABIN7227992)

Target: Complement C2

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Complement C2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-Complement C2 Antibody

Purpose: CO2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of CO2 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human CO2 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for Complement C2

Target: Complement C2

Alternative Name: CO2

Background: Rabbit Anti-CO2 Polyclonal Antibody,Complement C2, C3/C5 convertase,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.,CO2

Molecular Weight: observerd band 82kDa

Gene ID: 717

UniProt: P06681