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anti-Human BTN2A1 Antibodies:
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Human Polyclonal BTN2A1 Primary Antibody for EIA, WB - ABIN950690
Benyamin, McRae, Zhu, Gordon, Henders, Palotie, Peltonen, Martin, Montgomery, Whitfield, Visscher: Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. in American journal of human genetics 2009
Show all 5 references for 950690
Human Monoclonal BTN2A1 Primary Antibody for ELISA - ABIN395751
Malcherek, Mayr, Roda-Navarro, Rhodes, Miller, Trowsdale: The B7 homolog butyrophilin BTN2A1 is a novel ligand for DC-SIGN. in Journal of immunology (Baltimore, Md. : 1950) 2007
Show all 5 references for 395751
A comparison of the allele frequencies or genotype distributions by the chi2 test revealed that rs6929846 of BTN2A1 was significantly associated with dyslipidemia.
BTN2A1 may be a susceptibility gene for myocardial infarction in Japanese individuals.
Genetic variants of APOA5 (show APOA5 Antibodies) and BTN2A1 may synergistically affect the prevalence of dyslipidemia in East Asian populations and of metabolic syndrome in Japanese individuals.
BTN2A1 may be a susceptibility gene for Type 2 diabetes in Japanese individuals
Results suggest that BTN2A1 may be a susceptibility gene for chronic kidney disease in Japanese individuals.
BTN2A1 may be a susceptibility gene for hypertension in Japanese individuals, with the T allele being related to high blood pressure.
associations of rs6929846 of butyrophilin subfamily 2 member A1 to myocardial infarction among individuals stratified by the absence or presence of hypertension, diabetes mellitus and chronic kidney disease
The relationship between rs6929846 of BTN2A1 or rs2569512 of ILF3 (show MMP4 Antibodies) and myocardial infarction is influenced by the serum concentrations of high density lipoprotein cholesterol and low density lipoprotein cholesterol, respectively.
Rather than interacting with T cells, butyrophilin BTN2A1 is recognized by DC-SIGN (show CD209 Antibodies) on immature monocyte-derived dendritic cells.
This gene is a member of the BTN2 subfamily of genes, which encode proteins belonging to the butyrophilin protein family. The gene is located in a cluster on chromosome 6, consisting of seven genes belonging to the expanding B7/butyrophilin-like group, a subset of the immunoglobulin gene superfamily. The encoded protein is an integral plasma membrane B box protein involved in lipid, fatty-acid and sterol metabolism. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
butyrophilin, subfamily 2, member A1
, butyrophilin subfamily 2 member A2
, butyrophilin subfamily 2 member A1-like
, butyrophilin subfamily 2 member A1
, butyrophilin, subfamily 2, member A2