C1413-1ML Display Image

Complement C7 deficient serum human, for complement assays

Code: C1413-1ML D2-231

Analysis Note

C7 is depleted by immunoadsorption as judged by a highly sensitive hemolytic assay.

Application

Complement C7 deficiencies in human...


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£258.00 1ML

Analysis Note

C7 is depleted by immunoadsorption as judged by a highly sensitive hemolytic assay.

Application

Complement C7 deficiencies in humans are rare, but often associated with recurrent infections by Neisseria spp. (such as meningitis). C7 deficiencies in patients with meningococcal meningitis have shown a mutation which results in an 11 bp deletion in exon 6 resulting in a premature stop codon. Additionally, research has suggested that screening of patients with systemic neisserial infection by CH50 or the APH-50 assay can reveal a C7 deficiency.

Physical form

Supplied as a solution in PBS, pH 7.4

biological sourcehuman
formsolution
Gene Informationhuman ... C7(730)
Quality Level200
shipped indry ice
storage temp.−70°C
technique(s)activity assay: suitable
UniProt accession no.P10643
Pack1ML
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