Rabbit Polyclonal LAE antibody. Suitable for WB, IHC-P and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human ACSM1 aa 1-300.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 20% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
WB | IHC-P | |
---|---|---|
Human | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500.00000 - 1/3000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/100.00000 - 1/1000.00000 | Notes - |
Catalyzes the activation of fatty acids by CoA to produce an acyl-CoA, the first step in fatty acid metabolism (PubMed:10434065). Capable of activating medium-chain fatty acids (e.g. butyric (C4) to decanoic (C10) acids), and certain carboxylate-containing xenobiotics, e.g. benzoate (PubMed:10434065). Also catalyzes the activation of lipoate to lipoyl-nucleoside monophosphate (By similarity). Activates lipoate with GTP at a 1000-fold higher rate than with ATP and activates both (R)- and (S)-lipoate to the respective lipoyl-GMP, with a preference for (R)-lipoate (By similarity).
BUCS1, LAE, MACS1, ACSM1, Acyl-CoA synthetase medium-chain family member 1, Benzoate--CoA ligase, Butyrate--CoA ligase 1, Butyryl-coenzyme A synthetase 1, Lipoate-activating enzyme, Middle-chain acyl-CoA synthetase 1, Xenobiotic/medium-chain fatty acid-CoA ligase HXM-B
Rabbit Polyclonal LAE antibody. Suitable for WB, IHC-P and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human ACSM1 aa 1-300.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 20% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
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The target LAE also known by some researchers as HXLM is a notable protein with a mass typically around 58 kDa. It is located throughout various tissues but shows high expression levels in the liver and kidneys. Specifically LAE is recognized for its binding affinity and interaction with several cellular substrates playing a direct role in various cellular activities. The protein's structural characteristics allow it to engage in essential biochemical reactions within the cell.
LAE contributes significantly to cellular metabolism and regulation processes. It is part of a multimeric complex where it functions collaboratively with other proteins to maintain cellular balance. LAE is involved in energy production and molecule conversion making it critical in supporting cells under stress conditions. Its complex formation aids in transporting molecules across the cell membrane linking it to essential cellular operations.
LAE interacts predominantly with the glycolysis and gluconeogenesis pathways. In these pathways it associates with the enzyme hexokinase assisting in glucose breakdown and synthesis. This protein's involvement ensures efficient energy circulation and utilization within the cell. Additionally LAE connects with phosphofructokinase in modulating pathway activities highlighting its influence on broader metabolic functions.
LAE has strong connections to diabetes and renal dysfunction. Dysregulation of this protein can result in abnormal glucose metabolism a hallmark of diabetic conditions. When linked to disorders LAE's relationship with insulin-like growth factor binding protein plays a part in managing glucose levels and kidney health. Such associations deepen the understanding of LAE's potential as a therapeutic target in treating metabolic and renal diseases.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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7.5% SDS PAGE
All lanes: Western blot - Anti-LAE antibody (ab151456) at 1/1000 dilution
Lane 1: Jurkat whole cell lysate at 30 µg
Lane 2: Raji whole cell lysate at 30 µg
Lane 3: THP1 whole cell lysate at 30 µg
Predicted band size: 65 kDa, 88 kDa
Immunohistochemical analysis of paraffin embedded U87 xenograft tissue labeling LAE with ab151456 at 1/500.
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