Comparison

GOAT ANTI HUMAN C4

Item no. 18-783-314024
Manufacturer GENWAY
Amount 1 ml
Category
Type Antibody
Specific against Human (Homo sapiens)
Host Goat
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-23783D
Similar products 18-783-314024
Available
Genway ID:
GWB-23783D
Specificity:
C4
Isotype:
Polyclonal IgG
Buffer Solution:
TRIS buffered saline pH7. 4
Preservative Stabilisers:
0. 09% Sodium Azide (NaN3)
Immunogen:
Purified human C4
Specificity:
Recognises human C4 a secreted protein that plays a central role in activation of the classical pathway of the complement system. C4 is split into its constituent components C4a and C4b by the C1-complex. All belong to the biochemical cascade that forms part of the innate immune system. Recommended Secondary Antibodies: Rabbit Anti Goat IgG (Fc)
Function:
C4 plays a central role in the activation of the classical pathway of the complement system. It is processed by activated C1 which removes from the alpha chain the C4a anaphylatoxin. The remaining alpha chain fragment C4b is the major activation product and is an essential subunit of the C3 convertase (C4b2a) and the C5 convertase (C3bC4b2a) enzymes of the classical complement pathway. Derived from proteolytic degradation of complement C4 C4a anaphylatoxin is a mediator of local inflammatory process. It induces the contraction of smooth muscle increases vascular permeability and causes histamine release from mast cells and basophilic leukocytes. Subunit structureCirculates in blood as a disulfide-linked trimer of an alpha beta and gamma chain. Subcellular locationSecreted. Post-translational modificationPrior to secretion the single-chain precursor is enzymatically cleaved to yield the non-identical chains (alpha beta and gamma). During activation the alpha chain is cleaved by C1 into C4a and C4b and C4b stays linked to the beta and gamma chains. Further degradation of C4b by C1 into the inactive fragments C4c and C4d blocks the generation of C3 convertase. N- and O-glycosylated. O-glycosylated with a core 1 or possibly core 8 glycan. Ref. 15Ref. 16Ref. 18Ref. 19Ref. 20Ref. 21
Polymorphism:
Human complement component C4 is polymorphic at two loci C4A and C4B. 13 alleles of C4A and 22 alleles of C4B have been detected. The allele shown here is C4A4. The C4A alleles carry the Rodgers (Rg) while the C4B alleles carry the Chido (Ch) blood group antigens. The C4A6 allotype is totally deficient in hemolytic activity. Involvement in diseaseDefects in C4A are the cause of complement component 4A deficiency (C4AD) [MIM:120810]. A rare defect of the complement classical pathway associated with the development of autoimmune disorders mainly systemic lupus with or without associated glomerulonephritis.
Miscellaneous:
C4A allotypes react more rapidly with the amino group of peptide antigens while C4B allotypes react more rapidly with the hydroxyl group of carbohydrate antigens. Sequence similaritiesContains 1 anaphylatoxin-like domain. Contains 1 NTR domain.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 ml
Available: In stock
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