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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 Antibodies (16) 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 ELISA Kits) 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 ELISA Kits) in whole saliva (show RAG1AP1 ELISA Kits) were identified.
AMY1 (show AMY1A ELISA Kits) copy number was significantly correlated with the variation observed in salivary amylase (show AMY ELISA Kits) production and enzyme activity but did not explain the majority of observed variation between individuals. AMY1 (show AMY1A ELISA Kits)-odd and AMY1 (show AMY1A ELISA Kits)-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 ELISA Kits) 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 ELISA Kits) rs11185098 genotype associated with higher amylase (show AMY ELISA Kits) activity may have greater loss of adiposity during low-calorie diet interventions.
higher levels of sAA (show SAA1 ELISA Kits) in EHS participants
Serum amylase (show AMY ELISA Kits) 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 ELISA Kits) 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 ELISA Kits)) modestly differentiated between mucinous and nonmucinous lesions, and amylase (show AMY ELISA Kits) 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 ELISA Kits) gene copy number is associated with high insulin (show INS ELISA Kits) 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