Noun:

লাইপেস,

lipase শব্দের বাংলা অর্থ এর উদাহরণ:

লাইপেস দুধের স্বাদ বিস্বাদ করে দিতে পারে ।

জন্য.সেই কোষথলি তারপর লাইসোসোমের সঙ্গে মিশে যায় যার মধ্যে লাইসোসোমাল আসিড লাইপেস নামের একটি উপসেচক থাকে যা কলেস্টেরল এস্টারকে হাইড্রলাইজ করে.কোষের মধ্যে ।

lipase's Usage Examples:

A lipase (/ˈlaɪpeɪs/, /-peɪz/) is any enzyme that catalyzes the hydrolysis of fats (lipids).

Endothelial lipase (LIPG) is a form of lipase secreted by vascular endothelial cells in tissues with high metabolic rates and vascularization, such as.

Triglyceride lipases (EC 3.

Monoacylglycerol lipase, also known as MAG lipase, acylglycerol lipase, MAGL, MGL or MGLL is an enzyme that, in humans, is encoded by the MGLL gene.

Lipoprotein lipase (LPL) (EC 3.

34) is a member of the lipase gene family, which includes pancreatic lipase, hepatic lipase, and endothelial lipase.

Gastric lipase, together with lingual lipase, comprise the two acidic lipases.

These lipases, unlike alkaline lipases (such as pancreatic lipase), do not.

Hepatic lipase (HL), also called hepatic triglyceride lipase (HTGL) or LIPC (for "lipase, hepatic"), is a form of lipase, catalyzing the hydrolysis of.

Lingual lipase is a member of a family of digestive enzymes called triacylglycerol lipases, EC 3.

Diacylglycerol lipase, also known as DAG lipase, DAGL or DGL, is a key enzyme in the biosynthesis of the endocannabinoid 2-arachidonoylglycerol.

Hormone-sensitive lipase (EC 3.

79, HSL), also previously known as cholesteryl ester hydrolase (CEH), sometimes referred to as triacylglycerol lipase, is an enzyme.

Bile salt-dependent lipase (or BSDL), also known as carboxyl ester lipase (or CEL) is an enzyme produced by the adult pancreas and aids in the digestion.

Lysosomal lipase is a form of lipase which functions intracellularly, in the lysosomes.

The primary function of lysosomal lipase is to hydrolyze lipids.

Lipoprotein lipase deficiency is a genetic disorder in which a person has a defective gene for lipoprotein lipase, which leads to very high triglycerides.

Lysosomal acid lipase deficiency (LAL deficiency or LAL-D), is an autosomal recessive inborn error of metabolism that results in the body not producing.

is preventing the absorption of fats from the human diet by acting as a lipase inhibitor, thereby reducing caloric intake.

Saliva contains digestive enzymes called amylase, and lingual lipase, secreted by the salivary glands and serous glands on the tongue.

pancreases or pancrelipase and pancreatin, are commercial mixtures of amylase, lipase, and protease.

Uptake of HDL2 is mediated by hepatic lipase, a special form of lipoprotein lipase found only in the liver.

Hepatic lipase activity is increased by androgens.

triglyceride lipase (ATGL).

Subsequently, hormone-sensitive lipase (HSL) catalyzes.

epithelial cells (from which DNA can be extracted), enzymes (such as amylase and lipase), antimicrobial agents such as secretory IgA, and lysozymes.

Synonyms:

gastric juice; gastric acid; enzyme;

Antonyms:

anticatalyst;