Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit
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- sELISA
Supplier Data
Sandwich ELISA - Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit (AB279730)
Positive Control.
HeLa cells were treated with Calyculin A. Cells were solubilzed at 4 x 107 cells/ml in Cell Lysate Buffer. Serial dilutions of lysates were analyzed in this ELISA.
- sELISA
Supplier Data
Sandwich ELISA - Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit (AB279730)
HeLa cells treated with/without Calyculin A.
HeLa cells were untreated or treated with Calyculin A. Cell lysates were analyzed using this phosphoELISA.
- sELISA
Supplier Data
Sandwich ELISA - Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit (AB279730)
Western Blot analysis of HeLa cells treated with/without Calyculin A.
HeLa cells were untreated or treated with Calyculin A. Cell lysates were analyzed using this western blot.
Reactivity data
Product details
Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit (ab279730) is a very rapid, convenient, and sensitive assay kit that can monitor the activation or function of important biological pathways in human cell lysates. By determining phosphorylated ACC1 protein in your experimental model system, you can verify pathway activation in your cell lysates. You can simultaneously measure numerous different cell lysates without spending excess time and effort in performing a Western Blotting analysis.
This Sandwich ELISA kit is an in vitro enzyme-linked immunosorbent assay for the measurement of human phospho-ACC1 and Total ACC1. An anti-pan ACC1 antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and ACC1 present in a sample is bound to the wells by the immobilized antibody and the wells are washed. In select wells, rabbit anti-phospho ACC1 antibody is added to detect phosphorylated ACC1. In the remaining wells, biotinylated anti-pan-ACC1 antibody is used to detect pan ACC1. After washing away unbound antibody, HRP-conjugated anti-rabbit IgG or HRP-Streptavidin is pipetted into the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of ACC1 (S79) or pan ACC1 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Acetyl Coenzyme A Carboxylase contributes to fatty acid synthesis and regulation of metabolism. ACC exists in two main isoforms ACC1 which is found mainly in lipogenic tissues and ACC2 which is associated with oxidative tissues. These isoforms form part of larger complexes within the cell interacting with other enzymes and proteins to regulate metabolic processes. ACC also affects the synthesis of long-chain fatty acids by regulating the amount of malonyl-CoA available as a building block.
Pathways
Acetyl Coenzyme A Carboxylase plays a role in the synthesis of fatty acids and their cellular metabolism. This enzyme is a component of the lipogenesis pathway where it transforms acetyl-CoA to malonyl-CoA a step critical for fatty acid elongation. ACC interacts with proteins such as fatty acid synthase to carry out its function within these metabolic pathways. Additionally malonyl-CoA produced by ACC serves as a regulator of carnitine palmitoyltransferase 1 integrating with the fatty acid oxidation pathway.
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