FCGR2A Antibody, HRP conjugated

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Product Specs

Buffer
**Preservative:** 0.03% Proclin 300
**Constituents:** 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
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Synonyms
FCGR2A; CD32; FCG2; FCGR2A1; IGFR2; Low affinity immunoglobulin gamma Fc region receptor II-a; IgG Fc receptor II-a; CDw32; Fc-gamma RII-a; Fc-gamma-RIIa; FcRII-a; CD antigen CD32
Target Names
Uniprot No.

Target Background

Function
FCGR2A (CD32) is a low-affinity receptor that binds to the Fc region of immunoglobulin gamma (IgG). This binding initiates cellular responses against pathogens and soluble antigens, primarily by promoting phagocytosis of opsonized antigens.
Gene References Into Functions
  1. CD32 expression serves as a marker of CD4+ T cell activation in individuals living with HIV. PMID: 30013105
  2. This research indicates that genetic variation in human neutrophil Fcgamma receptors and SIRPalpha influences antibody-dependent cellular cytotoxicity towards cancer cells. PMID: 28952147
  3. This study highlights the impact of FCGR genetic polymorphism on antibody responses to GARP in patients with breast cancer. PMID: 29879453
  4. Data suggests that FC gamma receptor FCGR2A polymorphisms do not significantly influence the response to rituximab in patients with immune thrombocytopenic purpura (ITP). PMID: 28856973
  5. Results revealed a significantly higher frequency of FC gamma receptor FCGR3A-158V allele in patients with immune thrombocytopenia (ITP) compared to control subjects. However, no significant differences were found in the genotype distribution or allele frequencies for FC gamma receptor FCGR2A-131H/R between patients and controls. PMID: 28942727
  6. Differently oxidized isolated subspecies can lead to both stronger and weaker binding and activation of the histidine variant of Fc fragment of IgG receptor IIa (FcgammaRIIa). PMID: 28988621
  7. CRP binds to surface CD32 (also known as FcgammaRII) on myeloma cells, activating a pathway mediated by the kinase p38 MAPK and the transcription factor Twist, which enhances the cells' secretion of osteolytic cytokines. PMID: 29233917
  8. FCGR2A single nucleotide polymorphism is linked to susceptibility to idiopathic nephrotic syndrome. PMID: 29155175
  9. The alphaIIb beta3 antagonist TMV-7/trimucrin prevents thrombosis without causing Fc receptor gamma-chain IIa-mediated thrombocytopenia. PMID: 28815933
  10. The expression levels of human FcgammaRIIB, but not FcgammaRIIA, were negatively correlated with serum levels of IgE in human asthma patients. PMID: 29597194
  11. When higher-affinity genotypes for FCGR2A, FCGR3A, and FCGR2C were considered together, they were associated with significantly increased tumor shrinkage and prolonged survival in response to HD-IL2. This is the first study to demonstrate associations between FCGR genotypes and outcome following HD-IL2 treatment. PMID: 27742794
  12. FcgammaRIIA and FcgammaRIIB both showed increased methylation levels in Kawasaki disease (KD) patients who underwent IVIG treatment. FcgammaRIIA expression influenced the IVIG treatment response in KD patients. The FcgammaRIIA/IIB mRNA expression ratio was higher in KD patients with coronary artery lesion formation. PMID: 27893416
  13. FCGR2A rs1801274 G-allele is associated with susceptibility to Kawasaki disease and Ulcerative colitis. PMID: 27270653
  14. Farletuzumab demonstrates enhanced binding to FCGR3A-158V high-affinity receptor and an enhanced clinical outcome in ovarian cancer patients with low baseline CA125 levels and at least one high-affinity allele of FCGR2A or FCGR3A. PMID: 29041009
  15. Inhibition of Abl/Src with bosutinib reduced FcgammaRIIA-mediated glomerular neutrophil accumulation and renal injury in experimental, crescentic anti-GBM nephritis. PMID: 28891817
  16. This study demonstrates that p.His167Arg, a KD-associated FCGR2A variant, acts as a susceptibility gene in males only. The gender differences associated with FCGR2A in KD provide new insights into KD susceptibility. PMID: 28886140
  17. Data suggests a mechanism where Toll-like receptors TLR7/8 signaling, through shedding of FcgRIIA, shifts neutrophil function from phagocytosis to a programmed necrosis pathway, neutrophil extracellular trap formation (NETosis). PMID: 28606989
  18. Gene copy number variation (CNV) of the PKLR, FCGR2A, FCGR2C, and FCGR3 genes is associated with malaria severity. These findings provide evidence for a role of CNV in host responses to malaria. PMID: 28605553
  19. This research indicated no association between FCGR2A polymorphisms in Guillain-Barre Syndrome in a Brazilian population. PMID: 27609290
  20. FCGR3A V and FCGR2A R allele carriers exhibit better responsiveness to anti-TNF-alpha therapy. This is a review article. PMID: 27490376
  21. Association between Fc gamma receptor IIA genetic polymorphisms and susceptibility to severe malaria anemia in children in western Kenya. PMID: 28427365
  22. This study identified a subpopulation of 0.012% of CD4 T cells that express CD32a and host up to three copies of HIV DNA per cell. This CD32a(+) reservoir was highly enriched in inducible replication-competent proviruses and can be predominant in some participants. The potential identification of CD32a(+) lymphocytes as the elusive HIV-1 reservoir could lead to insights that facilitate specific targeting and elimination of this reservoir. PMID: 28297712
  23. Single nucleotide polymorphisms (SNPs) rs2099684 in IgG receptors FCGR2A/FCGR3A can be considered a genetic risk factor for Takayasu arteritis (TA) in the Chinese Han population. PMID: 27769046
  24. The mutant homozygote (CC) of the FCGR2A gene (rs1801274) may have a protective role among Chinese patients with UC. PMID: 27984611
  25. This is a review/meta-analysis suggesting that FcgammaRIIa-H131R may modify treatment response to rituximab in diffuse large B cell lymphoma. PMID: 28039707
  26. FCGR2A and FCGR2C polymorphisms may also contribute to immunocomplexemia present in sarcoidosis. PMID: 26801149
  27. The absence of TULA-2 and the relative level of TULA-2 expression modulate FcgammaRIIA-mediated platelet reactivity and heparin-induced thrombocytopenia in vivo. PMID: 27765766
  28. FCGR2A expression is significantly upregulated in human masticatory mucosa during wound healing. PMID: 28005267
  29. This is a review/meta-analysis suggesting that rheumatoid arthritis patients with FCGR2A HH + HR genotype show a poor response to adalimumab. PMID: 27074847
  30. Our findings indicate that CD16 158F>V polymorphism may contribute to the increased risk of Idiopathic Thrombocytopenic Purpura, whereas CD32 131H>R polymorphism may not be a significant risk factor for Idiopathic Thrombocytopenic Purpura. PMID: 27315784
  31. Our observations support the existence of a central FcgammaRIIA-mediated pathway through which human platelets respond to both Gram-negative and Gram-positive bacteria. PMID: 27025455
  32. FcgammaRIIA H131 allele and FcgammaRIIA H/H131 genotype were significantly increased in pediatric Guillain-Barre syndrome patients. PMID: 27064330
  33. FCGR2A/FCGR3A-related immune disorder might contribute to the etiology of Takayasu arteritis. PMID: 26996483
  34. Data indicates no significant difference in the allele or genotype frequencies of the Fcgamma2RA protein (FCGR2A) rs1801274 single nucleotide polymorphism observed between groups. PMID: 27267995
  35. The RR, HR, and HH FCGR2A-131 genotypes were detected in 1 (11%), 5 (56%), and 3 (33%) of patients with disease relapse compared to 25 (21%), 56 (47%), and 38 (32%) of the 119 patients without relapse. PMID: 27376362
  36. The data suggests that FcgammaRIIA genotyping can be used as a marker of genetic susceptibility to sepsis. PMID: 26490967
  37. FCGR3A and FCGR2A SNPs do not confer differential responsiveness to rituximab. PMID: 26510856
  38. Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis. PMID: 26748351
  39. R/R genotype of FCGR2A p.R131H and G/G genotype of CCL2 c.-2518 A > G polymorphisms are associated with thrombocytopenia, which is a characteristic laboratory finding in dengue infections. PMID: 26429304
  40. Genetic variants of rs6671847 at FCGR2A and rs17085007 at 13q12 conferred a risk of relapse in patients with ulcerative colitis. PMID: 25787843
  41. This research did not find a significant association between FCGR2A H131R and clinical outcome in KRAS wild metastatic colorectal cancer individuals with adjuvant cetuximab therapy. PMID: 26363448
  42. The results demonstrate an association between FcgRIIa, TNF-alpha, and IL-6 gene single nucleotide polymorphisms and symptom persistence in Dengue patients. PMID: 26429310
  43. FCGR2A polymorphisms constitute a risk factor for graft loss following kidney transplantation, and this effect is related to anti-HLA antibodies. PMID: 26429312
  44. FcgammaRIIIA/FcgammaRIIA gene polymorphisms and HER-2 may play a role in antibody-dependent cellular cytotoxicity and clinical response to trastuzumab in breast cancer. PMID: 26450443
  45. The study aimed to develop a novel method for Y402H (g.43097C>T) genotyping, confirm its association with AMD in the Greek population, and investigate the H131R polymorphism in AMD. PMID: 25811666
  46. These include an FCGR2A/2C chimeric gene that causes decreased expression. PMID: 26133275
  47. Genetic variation in Fc gamma receptor IIA may contribute to infectious susceptibility in trauma patients. PMID: 26496101
  48. This meta-analysis suggests that the H131R polymorphism in the FCGR2A gene might be associated with susceptibility to KD in Asians. PMID: 26125827
  49. The study found that homozygous carriers of the FcgammaRIIA-131R/R allele had higher malaria-specific antibody levels compared to heterozygous carriers of FcgammaRIIA-131R/H alleles and homozygous carriers of FcgammaRIIA-131H/H alleles. The pre-existing antibody responses were related to reduced subsequent risk of clinical malaria. PMID: 25447268
  50. This is a review discussing the role of human FCGR2A in immune processes and thrombosis. PMID: 25900780

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Database Links

HGNC: 3616

OMIM: 146790

KEGG: hsa:2212

STRING: 9606.ENSP00000271450

UniGene: Hs.352642

Subcellular Location
Cell membrane; Single-pass type I membrane protein.
Tissue Specificity
Found on monocytes, neutrophils and eosinophil platelets.

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