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The human complement C4 gene (C4A and C4B genes) locus is located in the highly polymorphic major histocompatibility complex (MHC) class III gene region on chromosome 6, which could be a short form (C4S, 14.6 kb) or a long form (C4L, 21 kb), depending on the absence or the presence of the 6.36 kb endogenous retroviral sequence HERV-K(C4) in.
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C4 varies in three key ways: copy number (CN), isoform, and length. C4 is the second gene in the four-gene RCCX cassette and positioned midway between the MHC class I and MHC class II gene clusters ().The RCCX cassette comprises STK19 (RP1), C4, CYP21A2, and TNXB ().CYP21A2 contains a recombination site resulting in mono-, bi-, and trimodular cassettes with one, two, and three functional.
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The c4 antisense RNA is a non-coding RNA used by certain phages that infect bacteria. It was initially identified in the P1 and P7 phages of E. coli. [2] The identification of c4 antisense RNAs solved the mystery of the mechanism for regulation of the ant gene, which is an anti-repressor. The c4 antisense RNA has two regions, called a' and b.
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Lane 1, 500 ng of pure C4 protein; lanes 2-4, loaded with 500 ng of purified C4α, C4β or C4γ chain respectively. (C) Sandwich ELISA to investigate the binding of vWFA-214 to C4/C4 chains shows the presence of a C4-binding site on the vWFA-214. The binding affinity of intact C2 and recombinant vWFA-214 protein to C4/C4 chains was nearly the.
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The confirm and further elucidate the role of the C4-binding site for C4, we used a substrate-blotting technique in which labeled C4 was incubated with nitrocellulose membrane-fixed C1s and its fragments. C4 was successfully blotted onto C1s and P1, but not P2-P4; i.e., further degradation of the L chain led to the loss of C4-binding.
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Background IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide and is an important cause of end-stage renal disease (ESRD). Exploring novel biomarkers is necessary for predicting the disease activity and progression of IgAN patients. The present study sought to investigate the value of serum C4 for predicting the prognosis of IgAN patients. Methods The primary endpoint of.
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Studies using synthetic oligonucleotides have shown that C4-AP incision by phosphodiesterases present in Escherichia coli is as efficient as that of a typical abasic site (AP). 11 Replication of C4′-oxidized abasic site by the Klenow exo − fragment of DNA polymerase I is also similar to an AP site. 12 However, single-stranded shuttle vector studies in E. coli revealed that replication of.
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The C4'-oxidized abasic site (C4-AP) is a commonly formed DNA lesion, which generates two types of interstrand cross-links (ICLs). The kinetically favored cross-link consists of two full length strands and forms reversibly and exclusively with dA. Cross-link formation is attributed to condensation of C4-AP with the N6-amino group of dA.
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We have predicted C4 beta-c F222-Y232 as a C2 binding site which we have termed the CRIT-ed1 domain, and the sequence [F/H]EVKX(4/5)P as a consensus C2-binding sequence. Anti-CRIT-ed1 cross-reacts with the C4 beta-chain and F222EVKITPGKPY232 appears to be the key epitope recognized by this Ab. Furthermore, anti-CRIT-ed1 was found to inhibit CP.
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The recombinant vWFA protein fixed on MagneHis Ni-Particles bound C4 in normal human serum. The C4 alpha, beta and gamma chains were separated by SDS/PAGE and purified separately by electro-elution. The purified C4 chains were then used in a sandwich ELISA, which showed the vWFA to bind C4 only via the C4beta chain.