LipoproteinsDigested lipidsVLDLPhospholipidsMetabolismAPOEAPOBRemnantsProteinsParticlesIntestinalProteinBloodstreamGolgiMain apolipoproteinVLDLsTriglycerideRemnantEnterocytesNascent chylomicronSmall intestinePresence of chylomicronsAccumulationLiverAbsorbed from the intestineFatsCompositionAdipose tissuePolyclonal AntibodyPrimarilyDensityHydrophilicNeurodegenerative diseasesMetabolicEmulsionsPolymorphismActivatesPlasmaFormationDyslipidemiaHumansGeneFattyDisorder characterizedAPOA4Thoracic
Lipoproteins25
- While circulating in blood, chylomicrons exchange components with high-density lipoproteins (HDL). (wikipedia.org)
- Plasma phospholipid levels are very low, while plasma apolipoprotein B, chylomicrons, very-low-density lipoproteins (VLDLs), and low-density lipoproteins (LDLs) are absent. (medscape.com)
- Jenny Kanter and Karin Bornfeldt of the University of Washington School of Medicine have shown previously that the low insulin levels characteristic of diabetes lead to increased levels of apolipoprotein C3, or APOC3, and triglyceride-rich lipoproteins, or TRLs, as well as accelerated atherosclerosis. (asbmb.org)
- Hyperlipidemia comprises a heterogeneous group of disorders, characterized by high levels in one or more lipids and/or lipoproteins [atherogenic free fatty acids (FA), triglycerides (TG) (hypertriglyceridemia), small dense low-density lipoprotein cholesterol (LDL-C) (hypercholesterolemia), and apolipoprotein (apo) B], and/or low level in antiatherogenic high density lipoprotein cholesterol (HDL-C), in the circulation [ 1 - 3 ]. (hindawi.com)
- Apolipoprotein A5 (apoA5) has been identified to play an important role in lipid metabolism, specifically in triglyceride (TG) and TG-rich lipoproteins (TRLs) metabolism. (biomedcentral.com)
- Lipids circulating in the bloodstream are transported in lipoproteins (contain hydrophilic apolipoproteins ) because the hydrophobic lipids are insoluble in plasma. (amboss.com)
- The major apolipoproteins of high-density lipoprotein (HDL) are alpha lipoproteins (ie, apolipoprotein A-I [apo A-I], apo A-II, apo A-IV), which are soluble and can move between different classes of lipoproteins. (medscape.com)
- The plasma lipoproteins include chylomicrons, very-low-density lipoproteins (VLDLs) , low-density lipoproteins (LDLs), and high-density lipoproteins (HDLs). (pharmacy180.com)
- Lipoproteins are composed of a neutral lipid (TAG, cholesteryl esters, or both) core surrounded by a shell of amphipathic apolipoproteins, phospholipid, and unesterified cholesterol. (pharmacy180.com)
- This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. (affbiotech.com)
- Apolipoprotein C-III (apo C-III) is found on the surface of triglyceride-rich lipoproteins ( 6 ). (docsopinion.com)
- The apolipoprotein (apo) content of chylomicrons and very low density lipoproteins was examined by isoelectric focusing. (utmb.edu)
- There are four primary lipoproteins: chylomicrons, very-low-density lipoproteins (VLDLs), low-density lipoproteins (LDLs), and high-density lipoproteins (HDLs). (layerorigin.com)
- Lipoproteins are complex particles with a central core containing cholesterol esters and triglycerides surrounded by free cholesterol , phospholipids , and apolipoproteins , which facilitate lipoprotein formation and function. (healthmatters.io)
- The main difference between chylomicrons and micelles is that chylomicrons are lipoproteins having a core of t riglycerides and cholesterols and a coat made of apolipoproteins and phospholipids , whereas micelles are globules of lipid molecules that are arranged in a spherical form in an aqueous solution. (pediaa.com)
- Chylomicrons are lipoproteins having a core of triglycerides and cholesterols and a coat of apolipoproteins and phospholipids. (pediaa.com)
- Moreover, chylomicrons are the largest of the lipoproteins. (pediaa.com)
- The 4 major lipoproteins are very low-density lipoprotein (VLDL), low-density lipoprotein (LDL), high-density lipoprotein (HDL), and chylomicrons (CMs). (medscape.com)
- Other apolipoproteins (A, C, D, E, and their subtypes) are soluble and are exchanged between lipoproteins during metabolism. (medscape.com)
- Apolipoproteins are proteins that have binding affinity for lipids to form packages called lipoproteins. (dnaaccesslab.com)
- The APOE gene encodes the Apolipoprotein E protein, which is a major component of chylomicrons and VLDLs (Very Low-Density Lipoproteins). (dnaaccesslab.com)
- The A apolipoproteins are the main form of protein found in high density lipoproteins (HDL), although APO A-I is also present in chylomicrons. (randox.com)
- Apolipoprotein E is the protein which allows recognition of these triglyceride wealthy lipoproteins by the liver cells and makes their elimination possible. (radiusguide.com)
- 2020-08-16 · The APOE gene provides instructions for making a protein called apolipoprotein E. This protein combines with fats (lipids) in the body to form molecules called lipoproteins. (web.app)
- Apolipoprotein E is the recognition site for receptors involved in the clearance of remnants of very low density lipoproteins and chylomicrons (summary by Blum, 2016). (web.app)
Digested lipids1
- It is important to note that, unlike digested carbohydrates (in the form of monosaccharides) and proteins (in the form of amino acids), digested lipids (in the form of chylomicrons) bypass the hepatic portal system, avoiding first pass metabolism. (wikipedia.org)
VLDL10
- PPAR-alpha activation increases the expression of lipoprotein lipase and apolipoprotein A-V (apoA-V) while simultaneously decreasing expression of apoC-III in the liver, which decreases VLDL particles and lowering plasma triglycerides in chylomicrons (Staels and Fruchart 2005). (bodybuilding.com)
- APOE is also involved in the formation of chylomicrons and VLDL and affects the activity of other lipid metabolism-associated proteins and enzymes, such as hepatic lipase and lipoprotein lipase. (dovepress.com)
- APOE is an integral component of chylomicrons, VLDL, and HDL in the peripheral system ( Table 1 ). (dovepress.com)
- Apolipoprotein B (apoB ) is a major component of atherogenic lipoprotein particles such as LDL, VLDL and Lp(a). (docsopinion.com)
- Chylomicron remnants, VLDL, IDL, LDL, and Lp (a) are all pro-atherogenic while HDL is anti-atherogenic . (healthmatters.io)
- MTP mediates intracellular lipid transport in the intestine and liver and thus ensures the normal function of chylomicrons (CMs) in enterocytes and of VLDL in hepatocytes. (medscape.com)
- Gemfibrozil also inhibits the synthesis and increases the clearance of apolipoprotein B, a carrier molecule for VLDL. (pharmfair.com)
- Apolipoprotein B is a major protein constituent of chylomicrons (apo B-48), LDL (apo B-100) and VLDL (apo B-100). (assaygenie.com)
- The microparticles described by Phillips and coworkers had a mean diameter of 24 nm, as judged by â ¦ Cholesterol also undergoes esterification as it is packaged into chylomicrons and VLDL inside intestinal and liver cells, respectively. (vondellhenderson.com)
- Apolipoprotein E spielt im Katabolismus von Chylomikronen, IDL und VLDL-Remnants wie auch von ApoE-reichem HDL eine wichtige Rolle. (web.app)
Phospholipids6
- These triglycerides, along with phospholipids and cholesterol, are added to apolipoprotein B48 to form immature chylomicrons. (wikipedia.org)
- The triglycerides are then combined with phospholipids, cholesteryl esters, and apolipoprotein B48 (ApoB48) to form a nascent chylomicron. (wikipedia.org)
- Chylomicron is a spherical particle with a core of triglycerides surrounded by a monolayer of phospholipids, cholesterol, and lipoprotein. (labpedia.net)
- Apolipoproteins B-48 and phospholipids are added. (amboss.com)
- These particles consist of a core of cholesterol esters and triglycerides surrounded by a monolayer of free cholesterol, phospholipids, and proteins (apolipoproteins). (medscape.com)
- These structures consist of an outer monolayer of protein (an Apolipoprotein) and polar lipids (phospholipids and unesterified cholesterol) plus an inner core of neutral lipids (triglycerides and cholesterol esters). (randox.com)
Metabolism12
- The distinct metabolism between large and small HDL indicates unique origins of human apolipoprotein A4. (harvard.edu)
- Differential associations between plasma concentrations of insulin and glucose and intestinal expression of key genes involved in chylomicron metabolism. (harvard.edu)
- Apo E (Apolipoprotein E) plays an important role in the metabolism of lipids in the plasma, and is also is a constituent of various plasma lipoprotein-lipid particles. (thermofisher.com)
- Lipid metabolism in the epidermis may be regulated by the expression of apolipoprotein E (APOE), a glycoprotein which is synthesized in a wide variety of extrahepatic tissues including skin [ 27 - 29 ]. (hindawi.com)
- The proteins, termed apolipoproteins, play an important role in lipoprotein metabolism. (medscape.com)
- these apolipoproteins have lipid-soluble segments, the beta apolipoproteins, which remain part of the lipoprotein throughout its metabolism. (medscape.com)
- The apolipoproteins interact with a series of enzymes and tissue receptors and are therefore responsible for further metabolism and catabolism of the micelle. (randox.com)
- The lipoprotein density and kind of apolipoproteins it contains determines the fate of the particle and its influence on metabolism. (radiusguide.com)
- Apolipoprotein (apo) E is a multifunctional protein with central roles in lipid metabolism, neurobiology, and neurodegenerative diseases. (web.app)
- Familial chylomicronemia syndrome (FCS) is a rare, autosomal recessive disorder of chylomicron metabolism that results from loss-of-function mutations within the genes that encode key checkpoint molecules in lipolysis. (ptcbio.com)
- The apolipoprotein contained in chylomicron emulsified by bile acid can improve the activity of lipoprotein lipase therby greatly increase the hydrolysis metabolism of fat. (rengty.net)
- Chylomicron-like lipid emulsions, resembling chylomicrons in composition, size and metabolism were prepared in the presence of [125 I]Aβ1-40. (iospress.com)
APOE13
- Once triglyceride stores are distributed, the chylomicron returns APOC2 to the HDL (but keeps APOE), and, thus, becomes a chylomicron remnant, now only 30-50 nm. (wikipedia.org)
- ApoB48 and APOE are important to identify the chylomicron remnant in the liver for endocytosis and breakdown. (wikipedia.org)
- Apolipoprotein E (APOE) gene variants have been reported to influence psoriasis risk. (hindawi.com)
- Apolipoprotein E (APOE) is a lipid-transport protein abundantly expressed in most neurons in the central nervous system. (dovepress.com)
- The apolipoprotein E (APOE) gene is located on chromosome 19 and encodes a glycoprotein that is 299 amino acids long. (dovepress.com)
- Apolipoprotein E (APOE) is a lipoprotein found primarily in chylomicrons and intermediate-density lipoprotein (IDL). (docsopinion.com)
- ApoE is one of over a dozen apoproteins and can be found on chylomicrons, VLDLs, and some HDLs. (layerorigin.com)
- Apolipoprotein E (apoE) is an important determinant for tile uptake of triglyceride-rich emulsions and lipuproteins hy the liver, and exerts affinity for both the LDL receptor (LDLr) and a distinct liver-specific recognition site. (zhangqiaokeyan.com)
- As these emulsions mimic chylomicrons, we anticipate that the apoE-dependent metabolic behavior of chylomicrons (remnants) is largely dependent on their size. (zhangqiaokeyan.com)
- Apolipoprotein E (ApoE) is expressed as Molecular Biology of Neurodegenerative Diseases. (web.app)
- APOE is an apolipoprotein, a protein associating with lipid particles, that mainly functions in lipoprotein-mediated lipid transport between organs via the plasma and interstitial fluids. (web.app)
- Apolipoprotein E (APOE) plays an important role in cholesterol transport and genetic variants in APOE have been linked to the risk of Alzheimer's disease. (web.app)
- APOE / Apolipoprotein E Protein LS-G39871 is a Recombinant Human APOE / Apolipoprotein E produced in Human Cells Lys19-His317 with 6His, C-terminus tag(s). (web.app)
APOB1
- Compared with control participants, in individuals with type 2 diabetes, chylomicron TG and ApoB-48 levels exhibited an approximately twofold higher response to the fat-rich meal, and a twofold higher increment was observed in ApoB-48 particles in the VLDL1 and VLDL2 density ranges (all p (bvsalud.org)
Remnants2
- When a large portion of the triglyceride core has been hydrolyzed, chylomicron remnants are formed and are taken up by the liver, thereby also transferring dietary fat to the liver. (wikipedia.org)
- We hypothesize that the periphery could be of importance for removal of the largest chylomicron remnants, as their size might partially exclude them penetrating the fenestrated hepatic sinusoidal endothelium to reach the hepatic chylomicron remnant receptors. (ox.ac.uk)
Proteins2
- Immature chylomicrons are transported from the smooth ER to the Golgi apparatus via SAR1B proteins, where they are processed, resulting in mature chylomicrons. (wikipedia.org)
- Hesse D, Jaschke A, Chung B, Schurmann A. Trans-Golgi proteins participate in the control of lipid droplet and chylomicron formation. (medlineplus.gov)
Particles6
- The primary translation product is a 396-residue preprotein which after proteolytic processing is secreted its primary site of synthesis, the intestine, in association with chylomicron particles. (joplink.net)
- Chylomicrons are the largest of the four particles and are constructed by the small intestine. (layerorigin.com)
- By analysis of the TRL subfractions, the RP removal was likely to be confined to the largest chylomicron remnant particles. (ox.ac.uk)
- Large chylomicrons have a diameter of about 1000 nm, while the smallest particles have a diameter of 75 nm to 200 nm. (pediaa.com)
- Chylomicrons" are the particles which ship fat to our physique's storage areas. (radiusguide.com)
- Chylomicrons are large, lipoprotein particles produced after a meal. (ptcbio.com)
Intestinal4
- Intestinal scavenger receptor class B type I as a novel regulator of chylomicron production in healthy and diet-induced obese states. (harvard.edu)
- A unique feature of APOA4 is that it is an intestinal apolipoprotein secreted on HDL and chylomicrons. (jci.org)
- Chylomicron forms in the endoplasmic reticulum of intestinal epithelial cells. (labpedia.net)
- Chylomicrons are assembled in intestinal mucosal cells from dietary lipids (primarily TAG). (pharmacy180.com)
Protein7
- A protein specific to chylomicrons is ApoB48. (wikipedia.org)
- The SAR1B gene provides instructions for making a protein that is needed for the transport of molecules called chylomicrons. (medlineplus.gov)
- Charcosset M, Sassolas A, Peretti N, Roy CC, Deslandres C, Sinnett D, Levy E, Lachaux A. Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein. (medlineplus.gov)
- APOA1, a secreted protein belonging to the apolipoprotein A1/A4/E family, participates in the reverse transport of cholesterol from tissues to the liver for excretion by promoting cholesterol efflux from tissues and by acting as a cofactor for the lecithin cholesterol acyltransferase (LCAT). (nih.gov)
- This protein is a major protein of plasma HDL and is also found in chylomicrons. (nih.gov)
- 1-3 Although individuals carrying the ε4 allele have higher and those carrying the Apolipoprotein (apo) E is a 299‐residue protein which functions as a key regulator of plasma lipid levels. (web.app)
- These genes encode apolipoprotein (apo) C-II and A-V, lipase maturation factor 1 (LMF1), and glycosylphosphatidylinositol-anchored high-density lipoprotein (HDL)-binding protein 1 (GPIHBP1). (ptcbio.com)
Bloodstream5
- Chylomicrons are needed to absorb fat-soluble vitamins and carry fats and cholesterol from the small intestine into the bloodstream . (medlineplus.gov)
- SAR1B gene mutations cause the retention of chylomicrons within enterocytes and prevent their release into the bloodstream. (medlineplus.gov)
- Absorbed lipids are transported in chylomicrons via the lymphatic system into the bloodstream, where they reach the liver , peripheral tissues (which have LDL receptors ) and adipose tissue (storage). (amboss.com)
- Apolipoprotein CII activates lipoprotein lipase, which is important in clearing chylomicrons from bloodstream. (medquizzes.net)
- Chylomicronemia is the accumulation in the bloodstream of chylomicrons. (ptcbio.com)
Golgi2
- Chylomicrons are made in the endoplasmic reticulum and later processed in the Golgi complex. (pediaa.com)
- Once in the enterocyte, FFA chains and 2MG compounds are transported to the endoplasmic reticulum, where they are reformed into triglycerides and packaged into chylomicrons in the golgi apparatus to receive chylomicron specific apolipoproteins, namely apo B48, which is a marker for TG chylomicron. (medscape.com)
Main apolipoprotein1
- The main apolipoprotein component is ApoB48. (wikipedia.org)
VLDLs4
- Following their clearance from the circulation, any triglycerides and cholesterol that remain inside the chylomicrons are repackaged into VLDLs by the liver and excreted into the circulation. (layerorigin.com)
- It promotes the clearance of chylomicrons and VLDLs from the circulation by allowing them to bind tightly to lipoprotein receptors on the surface of liver cells. (layerorigin.com)
- This is, in part, why chylomicrons and VLDLs have such short half-lives compared to LDLs. (layerorigin.com)
- Chylomicrons are degraded, VLDLs are converted to LDLs, and LDLs are converted to HDL. (pharmfair.com)
Triglyceride3
- Chylomicrons transport lipids absorbed from the intestine to adipose, cardiac, and skeletal muscle tissue, where their triglyceride components are hydrolyzed by the activity of the lipoprotein lipase, allowing the released free fatty acids to be absorbed by the tissues. (wikipedia.org)
- Once on chylomicrons, APOC2 activates triglyceride lipolysis and uptake via lipoprotein lipase (LPL) on peripheral tissues (step 5). (jci.org)
- Triglyceride is the major component of the chylomicron. (labpedia.net)
Remnant1
- The three stages of the chylomicron are nascent, mature, and remnant. (wikipedia.org)
Enterocytes1
- These chylomicrons exit the enterocytes by exocytosis. (pediaa.com)
Nascent chylomicron1
- Each nascent chylomicron particle has one molecule of apolipoprotein (apo) B-48. (pharmacy180.com)
Small intestine4
- This evidence supports the notion that APOA4 on small HDL originates directly from the small intestine while APOA4 on large HDL originates from chylomicron transfer. (jci.org)
- Chylomicron is in particulate form of lipoprotein, which is responsible for transporting exogenous cholesterol and triglycerides from the small intestine to the adipose tissue after the meal. (labpedia.net)
- Chylomicron is responsible for transporting the dietary fats from the small intestine to the tissue-like adipose, cardiac and skeletal muscles. (labpedia.net)
- Chylomicrons transport hydrophobic lipids from the small intestine to adipose, skeletal, and cardiac muscle tissue, while micelles help in the absorption of lipids and fat-soluble vitamins such as vitamins A, K, D, and E. (pediaa.com)
Presence of chylomicrons2
- The hyperchylomicronemia syndrome is a disorder characterized by extreme hypertriglyceridemia, the presence of chylomicrons, and one or more of the following clinical manifestations: eruptive xanthomas, lipaemia retinalis, hepatosplenomegaly, recurrent abdominal pain, and/ or acute pancreatitis. (wikipedia.org)
- In a fasting plasma sample, the presence of chylomicrons is indicated by a 'creamy' appearance. (ptcbio.com)
Accumulation5
- Patients with a deficiency of LPL or apo C-II show a dramatic accumulation of chylomicrons in the plasma (type I hyperlipoproteinemia, or familial LPL deficiency) even if fasted. (pharmacy180.com)
- Deficiency of this enzyme prevents affected individuals from properly digesting certain fats and results in massive accumulation of fatty droplets called chylomicrons in the circulation (chylomicronemia) and consequently also an increase of the plasma concentration of fatty substances called triglycerides. (digestivetracthealth.com)
- Chylomicronemia syndrome is a general term for the symptoms that develop due to the accumulation of chylomicrons in the plasma. (digestivetracthealth.com)
- Thus, chylomicrons not only aid in the distribution of dietary triglycerides but also assist in preventing their accumulation in the body. (pediaa.com)
- These mutations affect the activity of the LPL enzyme, resulting in accumulation of chylomicrons in the plasma. (ptcbio.com)
Liver3
- The chylomicrons with APOA4 then enter circulation (step 2), where APOA4 is exchanged for APOC2 on liver-derived large HDL (step 3), generating APOA4-containing large HDL (step 4). (jci.org)
- With a half-life of 15 to 20 minutes, chylomicrons are rapidly cleared from the blood by the liver. (layerorigin.com)
- The remaining fat molecules are absorbed by chylomicrons, which then transport them to the liver. (pediaa.com)
Absorbed from the intestine1
- Chylomicrons carry fat absorbed from the intestine. (hopkinsguides.com)
Fats4
- Chylomicron retention disease is an inherited disorder that impairs the normal absorption of fats, cholesterol, and certain vitamins from food. (medlineplus.gov)
- Impaired chylomicron transport causes severely decreased absorption (malabsorption) of dietary fats and fat-soluble vitamins, leading to nutritional and developmental problems in people with chylomicron retention disease. (medlineplus.gov)
- Chylomicron transport fats to adipose tissue and muscles. (labpedia.net)
- The primary function of chylomicrons is to deliver fats to organs to support tissue energy production in the post-prandial (fed) state. (layerorigin.com)
Composition1
- Each lipoprotein is characterized by its lipid composition and by the type and number of apolipoproteins it possesses. (medscape.com)
Adipose tissue1
- Chylomicrons also play a crucial role in the transportation of dietary triglycerides to skeletal muscles and adipose tissue. (pediaa.com)
Polyclonal Antibody1
- The following product was used in this experiment: Apolipoprotein E Polyclonal Antibody from Thermo Fisher Scientific, catalog # BS-4892R. (thermofisher.com)
Primarily3
- Nascent chylomicrons are composed primarily of triglycerides (85%) and contain some cholesterol and cholesteryl esters. (wikipedia.org)
- The features of chylomicron retention disease primarily affect the gastrointestinal system and nervous system. (medlineplus.gov)
- The commonest type of hyperlipidemia is postprandial hyperlipidemia, which is noticed after an animal consumes a meal containing fat and is due primarily to increased chylomicron ranges. (radiusguide.com)
Density1
- Apo E also plays an important role in the formation of very low density lipoprotein and chylomicrons. (thermofisher.com)
Hydrophilic3
- During this transport process, lipids are bound to special hydrophilic apolipoproteins . (amboss.com)
- In brief, chylomicrons and micelles are fat globules having a hydrophobic core and a hydrophilic coat. (pediaa.com)
- Bile acid have biosurfactant amphiphilic molecule structure with hydrophilic (hydroxyl, carboxyl) and hydrophobic (alkyl), have strong surface activity, which can effectively emulsifies fat into lipid droplets or chylomicron and improves the solubility of insoluble substances such as cholesterol in water. (rengty.net)
Neurodegenerative diseases1
- Apolipoprotein E Abnormal Function of Metalloproteins Underlies Most Neurodegenerative Diseases. (web.app)
Metabolic1
- In recent years, a newly discovered apolipoprotein has been proved to be closely related to the occurrence of obesity and metabolic syndrome. (biomedcentral.com)
Emulsions1
- The chylomicron-like emulsions containing Aβ were then injected into a lateral ear vein of conscious rabbits and blood sampled at regular intervals up to … 30 mins. (iospress.com)
Polymorphism1
- The apolipoprotein E polymorphism and the cholesterol-raising effect of coffee. (web.app)
Activates2
- Apo C-II activates endothelial lipoprotein lipase (LPL), which degrades the TAG in chylomicrons to fatty acids and glycerol. (pharmacy180.com)
- Apolipoprotein CII activates lipoprotein lipase. (medquizzes.net)
Plasma3
- 885 mg/dL]) and the abnormal persistence of chylomicrons in fasting plasma. (ptcbio.com)
- Lipoprotein lipase (LPL) clears chylomicrons from the plasma by hydrolysing the triglycerides into fatty acids and glycerol. (ptcbio.com)
- 1 In FCS, chylomicron clearance from plasma is impaired due to genetic mutations that affect LPL enzyme activity. (ptcbio.com)
Formation1
- Apolipoprotein (apo) B-48 is important for the formation of chylomicrons. (labpedia.net)
Dyslipidemia1
Humans1
- Apolipoprotein A4's (APOA4's) functions on HDL in humans are not well understood. (jci.org)
Gene2
- Mutations in a gene called SAR1B cause chylomicron retention disease. (medlineplus.gov)
- Recombinant Human Apolipoprotein B-100 is produced by our E.coli expression system and the target gene encoding Glu28-Ser127 is expressed with a 6His tag at the N-terminus. (assaygenie.com)
Fatty1
- Triglycerides of chylomicrons are hydrolyzed by LPL, and free fatty acids are released. (medquizzes.net)
Disorder characterized1
- Type I is a rare disorder characterized by severe elevations in chylomicrons and extremely elevated triglycerides, always reaching well above 1000 mg/dL and not infrequently rising as high as 10,000 mg/dL or more. (medscape.com)
APOA41
- APOA4 is synthesized and secreted into the lymph on the surface of chylomicrons (step 1). (jci.org)
Thoracic1
- Chylomicrons do not enter the portal system but go to the lymphatic system and thoracic duct. (labpedia.net)