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Chicken Monoclonal SREBF1 Primary Antibody für SimWes, WB - ABIN153469
Yin, Zhang, Hillgartner: Sterol regulatory element-binding protein-1 interacts with the nuclear thyroid hormone receptor to enhance acetyl-CoA carboxylase-alpha transcription in hepatocytes. in The Journal of biological chemistry 2002
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Cow (Bovine) Polyclonal SREBF1 Primary Antibody für ICC, IF - ABIN151638
Johnston-Cox, Koupenova, Yang, Corkey, Gokce, Farb, LeBrasseur, Ravid: The A2b adenosine receptor modulates glucose homeostasis and obesity. in PLoS ONE 2012
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Human Monoclonal SREBF1 Primary Antibody für EMSA, IP - ABIN2668814
Daniëls, Smans, Royaux, Chypre, Swinnen, Zaidi: Cancer cells differentially activate and thrive on de novo lipid synthesis pathways in a low-lipid environment. in PLoS ONE 2014
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Human Polyclonal SREBF1 Primary Antibody für ICC, IF - ABIN4355907
Dahlhoff, Worsch, Sailer, Hummel, Fiamoncini, Uebel, Obeid, Scherling, Geisel, Bader, Daniel: Methyl-donor supplementation in obese mice prevents the progression of NAFLD, activates AMPK and decreases acyl-carnitine levels. in Molecular metabolism 2014
Cow (Bovine) Polyclonal SREBF1 Primary Antibody für ICC, IF - ABIN4355909
Johnson, McDowell, Viereck, Xia: Species-specific dibutyl phthalate fetal testis endocrine disruption correlates with inhibition of SREBP2-dependent gene expression pathways. in Toxicological sciences : an official journal of the Society of Toxicology 2011
FTO (zeige FTO Antikörper) increased the lipid accumulation in hepatocytes by increasing nuclear translocation of SREBP1c and SREBP1c maturation, thus improving the transcriptional activity of lipid droplet-associated protein (zeige PLIN1 Antikörper) CIDEC (zeige CIDEC Antikörper).
common SNPs (rs62064119, rs2297508, rs11868035 and rs13306741) in the SREBP-1c gene were selected and genotyped in 593 Han patients with NAFLD and 593 healthy controls. No significant differences in genotype and allele frequencies of these four SNPs were found between cases and controls, suggesting that the SNPs are not associated with risk of NAFLD in the Chinese Han population.
Data suggests that expression of CYP4F2 (zeige CYP4F2 Antikörper) is down-regulated in liver of mice with non-alcoholic fatty liver disease after high-fat/Western diet and in human hepatocyte cell line exposed to excess palmitic acid, oleic acid, or fructose. Two other genes are down-regulated, PPAR gamma (zeige PPARG Antikörper) and SREBP-1. (CYP4F2 (zeige CYP4F2 Antikörper) = cytochrome P450 (zeige CYP Antikörper) family 4 subfamily F member 2; PPAR (zeige PPARA Antikörper) = peroxisome proliferator-activated receptor (zeige PPARD Antikörper) )
LncARSR promotes hepatic lipogenesis via Akt (zeige AKT1 Antikörper)/SREBP-1c pathway and contributes to the pathogenesis of nonalcoholic steatohepatitis.
CpG sites located in SREBF2 (zeige SREBF2 Antikörper) gene showed differential methylation in association with lipid traits. The expression of SREBF1 gene was inversely associated with methylation of its corresponding CpGs. Genetic variants in SREBF1 were also associated with lipid profile. SREBF1 expression was directly associated with HDL (zeige HSD11B1 Antikörper) cholesterol.
Epidermal growth factor receptor (EGFR (zeige EGFR Antikörper)) signaling enhances miR (zeige MLXIP Antikörper)-29 expression in glioblastoma cells via upregulation of Sterol regulatory element binding protein
Intracranial GBM xenografts were used to determine the effects of genetically silencing SOAT1 (zeige SOAT1 Antikörper) and SREBP-1 on tumor growth.
Our finding reveals a crucial roles for SREBP1 in lipid desaturation of ccRCC through regulation of NF-kappaB (zeige NFKB1 Antikörper) signaling, which provides not only new insights in regulatory mode of NF-kappaB (zeige NFKB1 Antikörper) signaling but also a novel target for potential metabolic therapies.
Our results suggest that relatively common genetic variants in stearoyl CoA desaturase (zeige SCD Antikörper) and SREBF1 attenuated the positive associations between intake of a traditional diet rich in n-3 polyunsaturated fatty acids and increases in fasting cholesterol and HbA1c levels, as well as the waist-to-hip ratio among Yup'ik participants.
changes in distinct lipid ratios may converge on ARF1 (zeige ARF1 Antikörper) to increase SBP-1 (zeige MEGF8 Antikörper)/SREBP-1 activity.
Data (including data from studies in transgenic/knockout mice) suggest that Kdm1a (zeige KDM1A Antikörper)-mediated attenuation of Srebf1 (zeige TOM1L2 Antikörper) transcriptional activities functions as underlying mechanism for suppression of de novo lipogenesis by oxidative stress in white adipose tissue. [Kdm1a (zeige KDM1A Antikörper) = lysine (K)-specific demethylase-1A (zeige KDM1A Antikörper); Srebf1 (zeige TOM1L2 Antikörper) = sterol-regulatory element-binding transcription factor-1]
Tlr4 (zeige TLR4 Antikörper)-mutant mice are resistant to acute alcohol-induced hepatic SREBP-1 activation and hepatic lipid accumulation.
Results showed that Glrx (zeige GRX1 Antikörper)(-/-) mice exhibited decreased SirT1 (zeige SIRT1 Antikörper) activity that leads to hyperacetylation and activation of SREBP-1 and upregulation of key hepatic enzymes involved in lipid synthesis.
Inhibition of NAMPT (zeige NAMPT Antikörper) aggravates high fat diet-induced hepatic steatosis in mice through regulating Sirt1 (zeige SIRT1 Antikörper)/AMPKalpha (zeige GRK4 Antikörper)/SREBP1 signaling pathway.
SREBP1 is dramatically reduced in dysbindin-1 (zeige DTNBP1 Antikörper) knockout mice; possibly related to cognitive deficits.
Epidermal growth factor receptor (EGFR (zeige EGFR Antikörper)) signaling enhances miR (zeige MLXIP Antikörper)-29 expression in glioblastoma cells via upregulation of Sterol regulatory element binding protein 1
The expression of hHL promoted hepatic triglyceride accumulation and de novo lipogenesis without affecting triglyceride secretion, and this was associated with an upregulation of Srebf1 (zeige TOM1L2 Antikörper) as well as the main genes controlling the synthesis of fatty acids. Transgenic mice also exhibited more adiposity and an increased LPL (zeige LPL Antikörper)-mediated FFA influx into the WAT without affecting glucose tolerance
Data show that miR (zeige MLXIP Antikörper)-200b and miR (zeige MLXIP Antikörper)-200c could directly bind the 3' UTR (zeige UTS2R Antikörper) of JUN (zeige JUN Antikörper), and JUN (zeige JUN Antikörper) activated the transcription of srebp1 to increase lipid accumulation.
a novel role for SREBP-1 as a cell surface retention factor for TbetaRI (zeige TGFBR1 Antikörper) in mesangial cells, is reported.
In vivo, the data of established transgenic animals showed that mice with lncHR1 expression had less hepatic expression of SREBP-1c, FAS (zeige FAS Antikörper), Acetyl-CoA carboxylase alpha (zeige ACACA Antikörper) (ACCalpha), and less hepatic and plasma TG after being fed a high-fat diet.
Polymorphisms of the ACACA (zeige ACACA Antikörper) and SREBF1 genes are promising markers for pig carcass and performance traits.
Results of associated analysis show that the polymorphism of ADD1 gene was associated traits of Intramuscular fat content (IMF (zeige MDFI Antikörper)) and back fat thickness (BF).
SREBF1 might play an important role in regulation of muscle fat deposition during postnatal growth of pigs.
SREBP1a activated while C/EBP (zeige CEBPA Antikörper) factors downregulated the activity of the SCD1 (zeige SCD Antikörper) promoter.
These results suggest that increased expression of hepatic CD36 (zeige CD36 Antikörper) and SREBP-1 is relevant in the obesity-driven lipid accumulation in the liver of dairy cows during late gestation.
Hepatic SREBP-1c-mediated lipid synthesis and the NF-kappaB (zeige NFKB1 Antikörper) inflammatory pathway were both overinduced in cows with fatty liver.
SREBP1 was found to be a key positive regulator of milk fat synthesis and was shown to be regulated by stearic acid and serum.
data suggest that low SREBP-1c expression can decrease lipid synthesis, increase lipid oxidation, and decrease the TG and VLDL content in bovine hepatocytes
84-bp indel in intron 5 was significantly associated with palmitoleic acid, stearic acid, saturated fatty acids, triglycerides and the C16 index in Simmental bulls.
genetic polymorphisms in sterol regulatory element binding transcription factor 1 (SREBF1)can be used to develop genetic tools for the selection of animals producing milk with healthier fatty acid composition
The results of this study demonstrated the existence of the polymorphisms in the SCD1 (zeige SCD Antikörper) and SREBP-1 genes in the population of Fleckvieh cattle and their associations with the concentrations of several muscle fat and subscutaneous fat fatty acids.
These results provide detailed genetic information for the SREBP1 signalling pathway and SCD (zeige SCD Antikörper) that can be used to change milk fat composition by marker-assisted breeding.
The SREBP1-9 SNP showed a significant effect on marbling score, monounsaturated fatty acids and C18 (zeige BBS9 Antikörper):1n-9 in the muscle fat of commercial Korean cattle.
the ability of Pu-erh (zeige ERH Antikörper) tea in promoting inhibition of food uptake and the biosynthesis of fat via SBP-1 and SCD (zeige SCD Antikörper), thereby reducing fat storage.
SBP-1/SREBP-1 is part of a conserved feedback loop responding to phosphatidylcholine (zeige SGMS1 Antikörper) levels to regulate expression of one-carbon cycle biogenesis genes and ensure adequate S-adenosylmethionine levels for phosphatidylcholine (zeige SGMS1 Antikörper) production.
elo-5 and elo-6 may be transcriptional targets of LPD (zeige ACSBG1 Antikörper)-1
both SBP-1 and MDT-15 control transcription of genes governing desaturation of stearic acid to oleic acid
Essential role of sbp-1 activation in oxygen deprivation induced lipid accumulation and increase in body width/length ratio in Caenorhabditis elegans.
This gene encodes a transcription factor that binds to the sterol regulatory element-1 (SRE1), which is a decamer flanking the low density lipoprotein receptor gene and some genes involved in sterol biosynthesis. The protein is synthesized as a precursor that is attached to the nuclear membrane and endoplasmic reticulum. Following cleavage, the mature protein translocates to the nucleus and activates transcription by binding to the SRE1. Sterols inhibit the cleavage of the precursor, and the mature nuclear form is rapidly catabolized, thereby reducing transcription. The protein is a member of the basic helix-loop-helix-leucine zipper (bHLH-Zip) transcription factor family. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Two transcript variants encoding different isoforms have been found for this gene.
, class D basic helix-loop-helix protein 1
, sterol regulatory element-binding protein 1
, adipocyte determination- and differentiation-dependent factor 1
, sterol regulatory element binding protein 1
, adipocyte determination and differentiation-dependent factor 1
, sterol regulatory binding transcription factor 1
, sterol regulatory element-binding transcription factor 1
, sterol regulatory element binding-protein 1
, sterol regulatory element binding transcription factor 1
, sterol response element binding protein 1
, similar to sterol regulatory element binding transcription factor 1 isoform b
, sterol regulatory element binding protein-1
, sterol regulatory element-binding protein 1-like
, Sterol regulatory element Binding Protein family member (sbp-1)
, Sterol regulatory element-binding transcription factor 1