ZNF550 MaxPab mouse polyclonal antibody (B01)
- Known as:
- ZNF550 MaxPab mouse pab (anti-) (B01)
- Catalog number:
- H00162972-B01
- Product Quantity:
- 50 uL
- Category:
- -
- Supplier:
- Abno
- Gene target:
- ZNF550 MaxPab mouse polyclonal antibody (B01)
Ask about this productRelated genes to: ZNF550 MaxPab mouse polyclonal antibody (B01)
- Gene:
- HCG18 NIH gene
- Name:
- HLA complex group 18
- Previous symbol:
- -
- Synonyms:
- FLJ31598, FLJ25550, Em:AB014087.1
- Chromosome:
- 6p22.1
- Locus Type:
- RNA, long non-coding
- Date approved:
- 2004-06-15
- Date modifiied:
- 2018-05-16
- Gene:
- HCG19P NIH gene
- Name:
- HLA complex group 19 pseudogene
- Previous symbol:
- -
- Synonyms:
- AB014085.4
- Chromosome:
- 6p21.3
- Locus Type:
- pseudogene
- Date approved:
- 2004-06-15
- Date modifiied:
- 2014-11-19
- Gene:
- PRR3 NIH gene
- Name:
- proline rich 3
- Previous symbol:
- -
- Synonyms:
- CAT56, Em:AB014077.1, Em:AB023052.2
- Chromosome:
- 6p21.33
- Locus Type:
- gene with protein product
- Date approved:
- 2003-05-21
- Date modifiied:
- 2016-10-05
- Gene:
- RANP1 NIH gene
- Name:
- RAN pseudogene 1
- Previous symbol:
- -
- Synonyms:
- Em:AB014080.2
- Chromosome:
- 6p22.1
- Locus Type:
- pseudogene
- Date approved:
- 2003-07-02
- Date modifiied:
- 2019-01-22
- Gene:
- RPP21 NIH gene
- Name:
- ribonuclease P/MRP subunit p21
- Previous symbol:
- C6orf135
- Synonyms:
- FLJ22638, Em:AB014085.3
- Chromosome:
- 6p22.1
- Locus Type:
- gene with protein product
- Date approved:
- 2003-06-02
- Date modifiied:
- 2016-10-05
Related products to: ZNF550 MaxPab mouse polyclonal antibody (B01)
Related articles to: ZNF550 MaxPab mouse polyclonal antibody (B01)
- Herpesviruses infect nearly all humans and have long been implicated in autoimmune and chronic diseases, yet their immune interactions with host proteins have not been systematically characterized at population scale. We profiled immunoglobulin G reactivities to >4,600 herpesvirus peptides and >15,000 human proteins using multiplexed protein display in two Mass General Brigham Biobank cohorts (discovery n=1,289; replication n=763), with longitudinal electronic health record follow-up. We identified and replicated 3,943 FDR-significant associations across 93 autoantigens, including previously uncharacterized viral-autoantigen axes, such as PHLDA1 and ZNF550. Eleven autoantigens were predicted by viral peptide reactivities with >85% accuracy in independent validation; some exhibited shared viral-host sequence homology, consistent with possible molecular mimicry. Integrating immune reactivities with incident disease outcomes revealed virus-specific network architectures: cytomegalovirus formed the largest multimorbid network, Epstein-Barr virus converged on pleiotropic autoimmune hubs, and herpes simplex viruses formed smaller, partially overlapping autoreactive networks. These findings define a herpesvirus-autoantigen-disease network atlas and prioritize candidate viral-host immune axes for mechanistic investigation. - Source: PubMed
Publication date: 2026/04/13
Lee SanghunPrince NicoleChen QingwenChen XueyingLu JunweiMendez Kevin MKelly Rachel SHecker JulianProkopenko DmitryMcGeachie Michael JSharma RinkuChen YuluAparicio AndreaGuo TaoLevy OferRattray Nicholas JwRattray ZahraLange ChristophLarman H BenjaminLasky-Su Jessica A