Anti-Human C4A/B Polyclonal Antibody

C4A (Complement C4A (Rodgers Blood Group)) is a Protein Coding gene. Diseases associated with C4A include C4a Deficiency and Immunodeficiency Due To A Classical Component Pathway Complement Deficiency. Among its related pathways are Complement Pathway and Innate Immune System. GO annotations related to this gene include endopeptidase inhibitor activity and complement component C1q binding. An important paralog of this gene is C4B. C4B (Complement C4B (Chido Blood Group)) is a Protein Coding gene. Diseases associated with C4B include C4b Deficiency and Immunodeficiency Due To A Classical Component Pathway Complement Deficiency. Among its related pathways are Innate Immune System and Complement Pathway. GO annotations related to this gene include carbohydrate binding and complement binding. An important paralog of this gene is C4A.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA06479
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the Internal region of human C4a/b.
Specificity Complement component C4 is expressed at highest levels in the liver, at moderate levels in the adrenal cortex, adrenal medulla, thyroid gland,and the kidney, and at lowest levels in the heart, ovary, small intestine, thymus, pancreas and spleen. The extra-hepatic sites of expression may be important for the local protection and inflammatory response.1 Publication
Isotype IgG
Reacitivity Human
Clone
Uniprot
Concentration 1mg/mL
Dilution WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000
Formulation
Application WB,IHC-p,ELISA
Other Names C4A,CO4,CPAMD2,Complement C4-A,Acidic complement C4,C3 and PZP-like alpha-2-macroglobulin domain-containing protein 2,C4B,CO4,CPAMD3,Complement C4-B,Basic complement C4,C3 and PZP-like alpha-2-macroglobulin domain-containing protein 3
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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