Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit (ab279730)
Key features and details
- Sample type: Cell Lysate
- Detection method: Colorimetric
- Assay type: Semi-quantitative
- Reacts with: Human
Overview
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Product name
Phospho-Acetyl Coenzyme A Carboxylase (S79) and Total Acetyl Coenzyme A Carboxylase ELISA Kit
See all Acetyl Coenzyme A Carboxylase kits -
Detection method
Colorimetric -
Sample type
Cell Lysate -
Assay type
Semi-quantitative -
Assay duration
Multiple steps standard assay -
Species reactivity
Reacts with: Human -
Product overview
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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Tested applications
Suitable for: Sandwich ELISAmore details -
Platform
Pre-coated microplate (12 x 8 well strips)
Properties
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Storage instructions
Store at -20°C. Please refer to protocols. -
Components 1 x 96 tests 20X Wash Buffer Concentrate 1 x 25ml 2X Cell lysate buffer 1 x 10ml 300X HRP-Streptavidin Concentrate 1 vial 5X Assay Diluent 1 x 15ml Biotinylated anti-pan-Acetyl Coenzyme A Carboxylase detection antibody 1 vial HRP-conjugated anti-rabbit IgG concentrate (1000X) 1 vial Pan-ACC1 Coated Microplate 1 unit Positive Control - treated HeLa cell lysate 1 vial Rabbit anti-phospho-Acetyl Coenzyme A Carboxylase (S79)-antibody 1 vial Stop Solution 1 x 8ml TMB One-Step Substrate Reagent 1 x 12ml -
Function
Catalyzes the rate-limiting reaction in the biogenesis of long-chain fatty acids. Carries out three functions: biotin carboxyl carrier protein, biotin carboxylase and carboxyltransferase. -
Tissue specificity
Expressed in brain, placental, skeletal muscle, renal, pancreatic and adipose tissues; expressed at low level in pulmonary tissue; not detected in the liver. -
Pathway
Lipid metabolism; malonyl-CoA biosynthesis; malonyl-CoA from acetyl-CoA: step 1/1. -
Involvement in disease
Acetyl-CoA carboxylase 1 deficiency -
Sequence similarities
Contains 1 ATP-grasp domain.
Contains 1 biotin carboxylation domain.
Contains 1 biotinyl-binding domain.
Contains 1 carboxyltransferase domain. -
Post-translational
modificationsPhosphorylation on Ser-1263 is required for interaction with BRCA1. -
Cellular localization
Cytoplasm. - Information by UniProt
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Alternative names
- ACAC
- ACACA
- ACACA_HUMAN
see all -
Database links
- Entrez Gene: 32 Human
- Entrez Gene: 31 Human
- Omim: 200350 Human
- Omim: 601557 Human
- SwissProt: O00763 Human
- SwissProt: Q13085 Human
- Unigene: 234898 Human
- Unigene: 160556 Human
Images
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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.
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HeLa cells were untreated or treated with Calyculin A. Cell lysates were analyzed using this phosphoELISA.
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HeLa cells were untreated or treated with Calyculin A. Cell lysates were analyzed using this western blot.