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anti-Human Fatty Acid Synthase Antibodies:
anti-Mouse (Murine) Fatty Acid Synthase Antibodies:
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Chicken Polyclonal Fatty Acid Synthase Primary Antibody for ICC, IF - ABIN152891
Gao, Bryzgalova, Hedman, Khan, Efendic, Gustafsson, Dahlman-Wright et al.: Long-term administration of estradiol decreases expression of hepatic lipogenic genes and improves insulin sensitivity in ob/ob mice: a possible mechanism is through direct regulation of signal ... in Molecular endocrinology (Baltimore, Md.) 2006
Show all 19 Pubmed References
Human Polyclonal Fatty Acid Synthase Primary Antibody for IF (p), IHC (p) - ABIN687382
Zhu, Luo, Wang, Yu, Wang, Shi, Sun, Lin, Li: Inhibition of FASN reduces the synthesis of medium-chain fatty acids in goat mammary gland. in Animal : an international journal of animal bioscience 2014
Show all 4 Pubmed References
Human Monoclonal Fatty Acid Synthase Primary Antibody for IF, IHC (p) - ABIN560848
Kristiansen, Rose, Geisler, Fritzsche, Gerhardt, Lüke, Ladhoff, Knüchel, Dietel, Moch, Varga, Theurillat, Gorr, Dahl: Endogenous myoglobin in human breast cancer is a hallmark of luminal cancer phenotype. in British journal of cancer 2010
Show all 3 Pubmed References
Human Monoclonal Fatty Acid Synthase Primary Antibody for IF, ELISA - ABIN560849
Oliveras-Ferraros, Vazquez-Martin, Fernández-Real, Menendez: AMPK-sensed cellular energy state regulates the release of extracellular Fatty Acid Synthase. in Biochemical and biophysical research communications 2008
Show all 2 Pubmed References
Human Polyclonal Fatty Acid Synthase Primary Antibody for ICC, IF - ABIN4310707
Huang, Bell, Okamura, Kim, Mohney, Guerrero-Preston, Ratovitski: Phospho-ΔNp63α/SREBF1 protein interactions: bridging cell metabolism and cisplatin chemoresistance. in Cell cycle (Georgetown, Tex.) 2012
Human Polyclonal Fatty Acid Synthase Primary Antibody for IHC (p), WB - ABIN3044520
Lu, Ma, Cai: Increased HAGLR expression promotes non-small cell lung cancer proliferation and invasion via enhanced de novo lipogenesis. in Tumour biology 2017
Fasn-1 regulates antimicrobial peptide (show CAMP Antibodies) nlp-29 expression in a WNK-1 (show WNK1 Antibodies) and gck (show GCK Antibodies)-3 dependent manner.
Genetic interactions at the cell-autonomous level, where glycolytic enzymes or Glo1 (show GLO1 Antibodies) were manipulated in FASN mutant cells, revealed that this sugar-dependent size reduction is a direct consequence of MG-derived-AGE accumulation
FASN-induced S6 kinase (show RPS6KB1 Antibodies) facilitates USP11 (show USP11 Antibodies)-eIF4B (show EIF4B Antibodies) complex formation for sustained oncogenic translation in diffuse large B-cell lymphoma.
HIV-1 infection increases intracellular levels of fatty acid synthase (FASN). Despite the requirement of FASN for nascent virion production, FASN activity was not required for intracellular Gag protein production, indicating that FASN dependent de novo fatty acid biosynthesis contributes to a late step of HIV-1 replication
Findings showed that FASN is upregulated in colorectal cancer cell lines that overexpress PGC-1alpha and indicated that FASN expression may enhance cancer cell proliferation by regulating antioxidant enzyme production and resistance to ROS-induced apoptosis. Further data provided evidence that FASN expression was regulated indirectly by PGC-1alpha.
Repression of FAS (show FAS Antibodies) mRNA expression is the consequence of feedback inhibition of FAS (show FAS Antibodies) expression by long chain fatty acyl-CoAs, which are formed by FACL3 (show Acsl3 Antibodies) during its upregulation by vitamin D3 in prostate cancer cells.
analysis of the expression of fatty acid synthase, Ki-67 (show MKI67 Antibodies) and p53 (show TP53 Antibodies) in squamous cell carcinomas of the larynx
Fatty acid synthase (FASN) mRNA and protein overexpression were associated with unfavorable clinicopathologic factors and poor outcomes.
KRAS is associated with activation of ERK2 (show MAPK1 Antibodies), induction of FASN, and promotion of lipogenesis.
The study has shown that the high frequency of FASN expression in intraepithelial neoplasia (hPIN)and cancer and no expression in most structures of benign hyperplasia make it possible to use this protein as an additional marker in the differential diagnosis of prostatic neoplasms.
FASN inhibition/knockdown significantly increased the susceptibility of cisplatin-resistant cells to NK cell cytotoxicity.
FASN has a role in leucine deprivation-inhibited proliferation and apoptosis of human breast cancer cells
FASN gene is a promising marker for subcutaneous fat tissue accumulation, while INSIG2 (show INSIG2 Antibodies) is a promising marker for FA composition
In this study, we investigated the FASN gene expression pattern and corresponding DNA methylation (show HELLS Antibodies) status in the inner layer of backfat from Jinhua pigs at different developmental stages.
calculated a 4.5 angstrom-resolution map of fatty acid synthase, and placed homologous template structures of all individual catalytic domains responsible for the cyclic elongation of fatty acid chains into the electron density
study determined fatty acid synthase crystal structure at 3.2 angstrom resolution covering five catalytic domains; structure reveals a complex architecture of alternating linkers and enzymatic domains
FASN regulates the pathogenicity of Th17 cells.
genetic deletion of FASN totally suppresses hepatocarcinogenesis driven by AKT and AKT/c-Met protooncogenes in mice.
Data show that nuclear factor Y (NF-Y) binds to the inverted CCAAT element (ICE) in the Fatty acid synthase (Fasn) promoter specifically in refeeding states.
study demonstrates that co-activation of AKT (show AKT1 Antibodies) and c-Met induces hepatocellular carcinoma development that depends on the mTORC1/FASN pathway.
Inhibition of G-protein-coupled Receptor Kinase 2 (show ADRBK1 Antibodies) Prevents the Dysfunctional Cardiac Substrate Metabolism in Fatty Acid Synthase Transgenic Mice.
These findings suggest that activation of TSHR (show TSHR Antibodies) directly inhibits FASN expression in mature adipocytes, possibly mediated by PKA and ERK (show EPHB2 Antibodies)
UCP2 (show UCP2 Antibodies)-induced fatty acid synthase promotes NLRP3 (show NLRP3 Antibodies) inflammasome activation during sepsis
FASN plays an important role in exercise-mediated cognitive enhancement, which might be associated to its role in modulating exercise-induced stimulation of neurogenesis.
FASN is essential for the development, functional competence, and maintenance of the lactating mammary gland.
Gamma-tocotrienol showed attenuation of triglyceride through effect on fatty acid synthase, sterol regulatory element-binding transcription factor 1 (show SREBF1 Antibodies), stearoyl CoA desaturase 1 (show SCD Antibodies), and carnitine palmitoyl transferase 1A gene expression in Hepa 1-6 cells.
FASN single nucleotide polymorphisms associated with milk fatty acids in a Chinese Holstein cattle.
g.841G>C SNP of FASN gene is associated with fatty acid composition in beef cattle.
Results indicate that Fatty acid synthase (FASN) may be used as a candidate gene affecting intramuscular fat content in Datong yaks.
It was suggested that two cattle breeds have an advantage in terms of genotype and haplotype distribution of the FASN gene; a single polymorphism might be a potential marker for breed discrimination.
study evaluated the contributions of polymorphisms of FASN and SCD (show SCD Antibodies) genes on fatty acid composition in muscle in two different populations: 1189 and 1058 Japanese Black cattle from the Miyagi and the Yamagata populations
The five exonic single nucleotide polymorphisms of g.12870, g.13126, g.15532, g.16907, and g.17924 in the FASN gene could change fatty acid contents.
Results suggest that SCD (show SCD Antibodies) and FASN are strong candidate genes influencing fatty acid composition in beef cattle.
The effects of genetic polymorphisms of liver X receptor, alpha (LXR (show NR1H3 Antibodies)), stearoyl-CoA desaturase (SCD (show SCD Antibodies)), Fatty acid synthase (FASN), and Fatty acid binding protein 4 (FABP4) were investigated on fatty acid composition in fat tissue of steers.
In ruminants, FASN may be regulated between the ratio between two transcripts. The small transcript is mostly produced in tissues with low fatty acid synthesis.
Polymorphisms within the FASN gene are associated with milk-fat content.
The results suggested that LXR (show NR1H3 Antibodies) regulates FASN promoter activity through direct interaction with the LXR (show NR1H3 Antibodies) response element as well as through increasing SREBP1 (show SREBF1 Antibodies) abundance.
The enzyme encoded by this gene is a multifunctional protein. Its main function is to catalyze the synthesis of palmitate from acetyl-CoA and malonyl-CoA, in the presence of NADPH, into long-chain saturated fatty acids. In some cancer cell lines, this protein has been found to be fused with estrogen receptor-alpha (ER-alpha), in which the N-terminus of FAS is fused in-frame with the C-terminus of ER-alpha.
fatty acid synthase
, fatty acid synthase Fas
, Fatty acid synthase Fas
, Fatty Acid SyNthase family member (fasn-1)
, fatty-acid synthase
, fatty-acid synthase II
, fatty-acid synthase fas
, fatty acid synthetase
, short chain dehydrogenase/reductase family 27X, member 1