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Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. Additionally we are shipping Amylase 1, Salivary Kits (27) and Amylase 1, Salivary Proteins (6) and many more products for this protein.
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our findings suggest that AMY1 copy number differences play a role in childhood-onset obesity but the effect differs between males and females.
Data indicate that the amylase (show AMY Antibodies) 1 (AMY1) copy number in an individual's genome is generally even and partially correlates with nearby single nucleotide polymorphism (SNPs), which do not associate with body mass index (BMI).
66 proteins that interact with amylase (show AMY Antibodies) in whole saliva (show RAG1AP1 Antibodies) were identified.
AMY1 (show AMY1A Antibodies) copy number was significantly correlated with the variation observed in salivary amylase (show AMY Antibodies) production and enzyme activity but did not explain the majority of observed variation between individuals. AMY1 (show AMY1A Antibodies)-odd and AMY1 (show AMY1A Antibodies)-even haplotypes showed a different relationship between copy number and expression levels, but the difference was not statistically significant.
Alcohol dependent patients showed significantly lower stress-related salivary alpha-amylase activity than healthy controls.
Results from 2 case-control cohorts of Chinese and Malays, show no previously reported association between AMY1 (show AMY1A Antibodies) and obesity or body mass index.
It was concluded that the genetic variant determining starch metabolism influences the response to weight-loss dietary intervention. Overweight and obese individuals carrying the AMY1-AMY2 (show AMY Antibodies) rs11185098 genotype associated with higher amylase (show AMY Antibodies) activity may have greater loss of adiposity during low-calorie diet interventions.
higher levels of sAA (show SAA1 Antibodies) in EHS participants
Serum amylase (show AMY Antibodies) levels in the normal range are positively associated with integrated islet beta cell function in patients with early type 2 diabetes.
Our findings suggest an effect of the interaction between starch intake and AMY1 (show AMY1A Antibodies) copy number on obesity. Individuals with high starch intake but low genetic capacity to digest starch had the lowest BMI, potentially because larger amounts of undigested starch are transported through the gastrointestinal tract, contributing to fewer calories extracted from ingested starch.
Data show that carcinoembryonic antigen (CEA (show CEACAM5 Antibodies)) modestly differentiated between mucinous and nonmucinous lesions, and amylase (show AMY Antibodies) did not distinguish intraductal papillary mucinous neoplasms (IPMNs) from mucinous cystadenomas (MCAs).
genetic association studies in a population of men in Republic of Korea: Data suggest that low AMY1A (show AMY1A Antibodies) gene copy number is associated with high insulin (show INS Antibodies) resistance and thus with genetic predisposition to diabetes type 2 and metabolic syndrome.
Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. The human genome has a cluster of several amylase genes that are expressed at high levels in either salivary gland or pancreas. This gene encodes an amylase isoenzyme produced by the salivary gland. Alternative splicing results in multiple transcript variants encoding the same protein.
1,4-alpha-D-glucan glucanohydrolase 1
, alpha amylase 1
, alpha-amylase 1
, salivary and hepatic alpha-amylase
, amylase 1, salivary
, amylase, salivary, alpha-1A
, salivary alpha-amylase
, salivary amylase alpha 1A