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anti-Human MTTP Antikörper:
anti-Mouse (Murine) MTTP Antikörper:
anti-Rat (Rattus) MTTP Antikörper:
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Mouse (Murine) Monoclonal MTTP Primary Antibody für IF, WB - ABIN968716
Chen, Newberry, Norris, Xie, Luo, Kennedy, Davidson: ApoB100 is required for increased VLDL-triglyceride secretion by microsomal triglyceride transfer protein in ob/ob mice. in Journal of lipid research 2008
Show all 6 Pubmed References
Cow (Bovine) Polyclonal MTTP Primary Antibody für WB - ABIN2781495
Lundahl, Skoglund-Andersson, Caslake, Bedford, Stewart, Hamsten, Packard, Karpe: Microsomal triglyceride transfer protein -493T variant reduces IDL plus LDL apoB production and the plasma concentration of large LDL particles. in American journal of physiology. Endocrinology and metabolism 2006
Show all 3 Pubmed References
two new hypolipidemic patients with very low plasma triglyceride and apolipoprotein B (apoB (zeige APOB Antikörper)) levels with plasma lipid profiles similar to abetalipoproteinemia (ABL (zeige ABL1 Antikörper)) patients, are reported.
results of this study, examining a cohort of obese children, suggest that the genetic variation at MTTP rs2306986 was associated with higher susceptibility to NAFLD (zeige TSC2 Antikörper)
Data suggest that amphipathic beta-strands in 200 N-terminal residues of beta1 domain of APOB (zeige APOB Antikörper) are required for secretion of lipid-rich or lipid-poor particles; residues 300-700 or 1050-1500 of beta1 domain appear to be required for secretion of lipid-rich particles; MTTP is required for secretion of intact APOB (zeige APOB Antikörper) but not of truncated APOB (zeige APOB Antikörper). (APOB (zeige APOB Antikörper) = apolipoprotein B (zeige APOB Antikörper); MTTP = microsomal triglyceride transfer protein)
In chronic hepatitis C patients infected with HCV genotype 3 and with the TT/GT genotype of the MTTP -493G/T SNP, a significant increase in hepatic steatosis was observed, which may indicate that this SNP has a significant influence on the accumulation of triglycerides in hepatocytes.
High expression of MTTP is associated with high carotid intima-media thickness.
MTP Gene Variants are associated with Homozygous Familial Hypercholesterolemia.
the N-terminal domain of MTP is important for its lipid transfer activity
These studies indicated that SAP18 (zeige SAP18 Antikörper) expression enhanced the recruitment of mSin3A in coordination with TRIB1 (zeige TRIB1 Antikörper) to MTTP regulatory elements and increased MTTP expression.
Results present evidence that MTTP polymorphisms could modulate the lipid homeostasis to determine the serum lipids and increase risk of non-alcoholic fatty liver disease.
Findings from meta-analysis indicate that the MTP -493G/T polymorphism may contribute to the development of non-alcoholic fatty liver disease. Thus, the MTP -493G/T polymorphism may be a biomarker for the early detection of the disease.
Microsomal triglyceride transfer protein protein plays a critical role in lipid droplet maturation, but does not regulate total body fat accumulation.
data provide the first in vivo evidence of the transcriptional regulatory activity of beta-apocarotenoids and identify microsomal triglyceride transfer protein and its transcription factors as the targets of their action. This study demonstrates that beta-carotene induces a feed-forward mechanism in the placenta to enhance the assimilation of beta-carotene for proper embryogenesis.
PHARMACOLOGICAL STUDY OF NEW COMPOUNDS ACTING AS REGULATORS OF 18-KDA TRANSLOCATOR PROTEIN (zeige TSPO Antikörper) LIGANDS
Intestine-specific MTP (zeige LAPTM4A Antikörper) and global ACAT2 (zeige SOAT2 Antikörper) deficiency lowers acute cholesterol absorption with chylomicrons and HDLs (zeige CSF1R Antikörper)
intestine-specific Mttp deletion is beneficial in young septic mice but harmful in aged mice
identified microsomal triglyceride transfer protein, which we show is also under the transcriptional regulation of C/EBPbeta (zeige CEBPB Antikörper) and -delta, as a novel player in the presentation of endogenous lipid antigens by adipocytes
effects of reducing either systemic or liver-specific MTP (zeige LAPTM4A Antikörper) activity on cholesterol metabolism and reverse cholesterol transport
Data show that combined deletion of microsomal triglyceride transfer protein (Mttp) and liver fatty acid binding protein 1 (L-Fabp (zeige FABP1 Antikörper)) are protected from lithogenic diet (LD)-induced gallstone formation.
FoxO6 (zeige Foxo6 Antikörper) is an important signaling molecule upstream of MTP (zeige LAPTM4A Antikörper) for regulating hepatic VLDL-TG production
intestinal MTP (zeige LAPTM4A Antikörper) and ABCA1 (zeige ABCA1 Antikörper) are critical for lipid absorption and are the main determinants of plasma and intestinal lipid levels.
promotes assembly and secretion of human apolipoprotein B (zeige APOB Antikörper)
the phospholipid transfer activity of MTP is sufficient for the assembly and secretion of primordial apoB (zeige APOB Antikörper) lipoproteins
Nonesterified fatty acids significantly inhibit the expression of ApoB100 (zeige APOB Antikörper), ApoE (zeige APOE Antikörper), MTP, and LDLR (zeige LDLR Antikörper), thereby decreasing the synthesis and assembly of VLDL and inducing TG accumulation in bovine hepatocytes.
after calving the apolipoprotein B(100 (zeige APOB Antikörper)) mRNA synthesis was lower, whereas microsomal triglyceride transfer protein (MTP) and apolipoprotein E (zeige APOE Antikörper) messenger RNA abundance were higher in the liver
measurements of the transfer of phospholipids (PLs (zeige CTSC Antikörper)) and cholesteryl esters (CEs)to acceptor vesicles by purified MTP showed TAG transfer activity was the most robust, and CE and PL transfer activities were 60-71% and 5-13% of the TAG transfer activity
MTTP is regulated by apo A-IV in manner to promote increased packaging of triglyceride into chylomicron core, which may be important in neonatal fat absorption.
There appears to be an interaction between the porcine MTTP genotype and the type of fat source in the pig diet, which would agree with the previous results on the biology of MTTP biology.
analysis of developmental expression and nutritional regulation of zebrafish homolog to mammalian microsomal triglyceride transfer protein large subunit
In a genetic study of lipid transport and metabolism, larval levels of microsomal triglyceride transfer protein (Mtp), the protein responsible for packaging triacylglycerol and beta-lipoproteins into lipoprotein particles, are unchanged by feeding.
MTP encodes the large subunit of the heterodimeric microsomal triglyceride transfer protein. Protein disulfide isomerase (PDI) completes the heterodimeric microsomal triglyceride transfer protein, which has been shown to play a central role in lipoprotein assembly. Mutations in MTP can cause abetalipoproteinemia.
microsomal triglyceride transfer protein (large polypeptide, 88kDa)
, microsomal triglyceride transfer protein large subunit
, microsomal triglyceride transfer protein B
, microsomal triglyceride transfer protein, large subunit
, microsomal triacylglycerol transfer protein
, microsomal triglyceride transfer protein