anti cfhr5 antibody Search Results



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Abnova rabbit anti-cfhr5 polyclonal antibody
Pedigree with familial C3 glomerulopathy demonstrating segregation of renal disease with mutant <t>CFHR5</t> protein. CFHR, complement factor H related.
Rabbit Anti Cfhr5 Polyclonal Antibody, supplied by Abnova, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+cfhr5+antibody/rabbit+monoclonal+anti+human+cfhr5+antibody/pmc03789233-84-20-24
Average 90 stars, based on 1 article reviews
rabbit anti-cfhr5 polyclonal antibody - by Bioz Stars, 2026-09
90/100 stars
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This gene is a member of a small complement factor H (CFH) gene cluster on chromosome 1. Each member of this gene family contains multiple short consensus repeats (SCRs) typical of regulators of complement activation.
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Recombinant Mouse Antibody Fab Fragment recognizes and reacts with Human CFHR5, expressed in Chinese Hamster Ovary cells(CHO).Formats of immunological tests: Immunoprecipitation; Neutralization; Functional Study≥1 year at -20°C. If the reconstituted antibody cannot be used within
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Involved in complement regulation.Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.http://www.creative-diagnostics.com/Anti-CFHR5-PAb-198170-147.htm
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Rabbit anti-Homo sapiens (Human) CFHR5 Polyclonal Antibody
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Involved in complement regulation.Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.http://www.creative-diagnostics.com/Anti-CFHR5-PAb-202576-147.htm
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Involved in complement regulation.Shipped at 4°C. Store at 4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle.http://www.creative-diagnostics.com/Anti-CFHR5-PAb-204107-147.htm
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Recombinant Mouse Antibody is capable of binding to Human CFHR5, expressed in Chinese Hamster Ovary cells(CHO).Formats of immunological tests: Enzyme-linked Immunosorbent Assay; Immunofluorescence; Functional Study4°C or -20°C, avoid repeated freezing and thawing.http://www.creativebiolabs.net/Rcombinant-Anti-Human-CFHR5-Antibody-5430.htm
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Pedigree with familial C3 glomerulopathy demonstrating segregation of renal disease with mutant CFHR5 protein. CFHR, complement factor H related.

Journal: Kidney International

Article Title: A novel CFHR5 fusion protein causes C3 glomerulopathy in a family without Cypriot ancestry

doi: 10.1038/ki.2013.348

Figure Lengend Snippet: Pedigree with familial C3 glomerulopathy demonstrating segregation of renal disease with mutant CFHR5 protein. CFHR, complement factor H related.

Article Snippet: The samples were run on standard 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis under nonreducing conditions and probed with a rabbit anti-CFHR5 polyclonal antibody (Abnova, Taipei City, Taiwan, cat. no. H30081494-DO1P).

Techniques: Mutagenesis

Characterization of the abnormal CFHR5 protein in the pedigree. ( a ) Western blot of serum with a polyclonal anti-human CFHR5 antibody. Both the normal CFHR5 protein and an abnormal higher-molecular-weight protein were detected in the index case and the serum of affected family members. ( b ) Schematic representation and chromatogram showing genomic breakpoint. The ACT sequence is common to both introns 1 and 3. The abnormal genomic amplicon was generated using the forward primer in intron 3 (green arrow, 5′-TATTGGCTGTGGGTTTGTCA-3′) and the reverse primer in intron 1 (red arrow, 5′-TGACTGATCACTTATATCACAGTTGG-3′). The breakpoint is 4583 bp into CFHR5 intron 3 (A of ACT=4584), where the sequence switches to CFHR5 intron 1 at 2797 (A of ACT=2798). ( c ) Screening for the genomic breakpoint by polymerase chain reaction. The 337-bp amplicon is amplified from the wild-type CFHR5 gene. If the intronic breakpoint is present, a 239-bp amplicon is generated. CFHR, complement factor H related.

Journal: Kidney International

Article Title: A novel CFHR5 fusion protein causes C3 glomerulopathy in a family without Cypriot ancestry

doi: 10.1038/ki.2013.348

Figure Lengend Snippet: Characterization of the abnormal CFHR5 protein in the pedigree. ( a ) Western blot of serum with a polyclonal anti-human CFHR5 antibody. Both the normal CFHR5 protein and an abnormal higher-molecular-weight protein were detected in the index case and the serum of affected family members. ( b ) Schematic representation and chromatogram showing genomic breakpoint. The ACT sequence is common to both introns 1 and 3. The abnormal genomic amplicon was generated using the forward primer in intron 3 (green arrow, 5′-TATTGGCTGTGGGTTTGTCA-3′) and the reverse primer in intron 1 (red arrow, 5′-TGACTGATCACTTATATCACAGTTGG-3′). The breakpoint is 4583 bp into CFHR5 intron 3 (A of ACT=4584), where the sequence switches to CFHR5 intron 1 at 2797 (A of ACT=2798). ( c ) Screening for the genomic breakpoint by polymerase chain reaction. The 337-bp amplicon is amplified from the wild-type CFHR5 gene. If the intronic breakpoint is present, a 239-bp amplicon is generated. CFHR, complement factor H related.

Article Snippet: The samples were run on standard 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis under nonreducing conditions and probed with a rabbit anti-CFHR5 polyclonal antibody (Abnova, Taipei City, Taiwan, cat. no. H30081494-DO1P).

Techniques: Western Blot, Molecular Weight, Sequencing, Amplification, Generated, Polymerase Chain Reaction