catalog number :
MBS857833
products full name :
ATP-Citrate Lyase (ACLY) Antibody
products short name :
[ATP-Citrate Lyase]
products name syn :
[ACL; ATPCL; CLATP]
other names :
[ATP-citrate synthase isoform 1; ATP-citrate synthase; ATP-citrate synthase; ATP citrate lyase; ATP-citrate (pro-S-)-lyase; ACL; Citrate cleavage enzyme]
products gene name :
[ACLY]
other gene names :
[ACLY; ACLY; ACL; ATPCL; CLATP; ACL]
specificity :
This antibody detects endogenous levels ATP-Citrate Lyase and does not cross-react with related proteins.
purity :
Affinity purified
form :
Purified mouse monoclonal in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50%, glycerol
tested application :
Western Blot (WB), Immunocytochemistry (ICC), Flow Cytometry (FC/FACS)
image1 heading :
Testing Data
image2 heading :
Testing Data #2
image3 heading :
Testing Data #3
other info1 :
Immunogen: Purified recombinant human ATP-Citrate Lyase protein fragments expressed in E Coli. Cellular Localization: Cytoplasm
products categories :
Autophagy antibody; Cancer; Cardiovascular; Cell Biology; Epigenetics & Nuclear Signaling; Developmental Biologys; Immunology; Drug Discovery Products; Metabolism; Neuroscience; Signal Transduction; Stem Cells
products description :
UniPort Summary Function: ATP citrate-lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. Has a central role in de novo lipid synthesis. In nervous tissue it may be involved in the biosynthesis of acetylcholine. Entrez Summary: ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440, 000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Two transcript variants encoding distinct isoforms have been identified for this gene.
ncbi acc num :
NP_001087.2
ncbi gb acc num :
NM_001096
ncbi pathways :
ChREBP Activates Metabolic Gene Expression Pathway (106104); Citrate Cycle (TCA Cycle) Pathway (82927); Citrate Cycle (TCA Cycle) Pathway (288); Fatty Acid Biosynthesis Pathway (198873); Fatty Acyl-CoA Biosynthesis Pathway (106115); Fatty Acid, Triacylglycerol, And Ketone Body Metabolism Pathway (160977); Integration Of Energy Metabolism Pathway (106096); Metabolism Pathway (477135); Metabolism Of Lipids And Lipoproteins Pathway (160976); SREBP Signalling Pathway (219802)
ncbi summary :
ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Dec 2014]
uniprot summary :
ATP-citrate synthase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. Has a central role in de novo lipid synthesis. In nervous tissue it may be involved in the biosynthesis of acetylcholine.