Goat Polyclonal Aldolase antibody - conjugated to HRP. Suitable for IP, WB and reacts with Rabbit, Human samples. Cited in 5 publications. Immunogen corresponding to Native Full Length Protein corresponding to Rabbit ALDOA.
Preservative: 0.01% Gentamicin sulphate
Constituents: 1% BSA, 0.88% Sodium chloride, 0.27% Tripotassium orthophosphate
IP | WB | |
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Human | Expected | Tested |
Mouse | Predicted | Predicted |
Rat | Predicted | Predicted |
Rabbit | Tested | Expected |
Species | Dilution info | Notes |
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Species Rabbit | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/500.00000 - 1/5000.00000 | Notes - |
Species | Dilution info | Notes |
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Species Rabbit | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
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Catalyzes the reversible conversion of beta-D-fructose 1,6-bisphosphate (FBP) into two triose phosphate and plays a key role in glycolysis and gluconeogenesis (PubMed:14766013). In addition, may also function as scaffolding protein (By similarity).
ALDA, ALDOA, Fructose-bisphosphate aldolase A, Lung cancer antigen NY-LU-1, Muscle-type aldolase
Goat Polyclonal Aldolase antibody - conjugated to HRP. Suitable for IP, WB and reacts with Rabbit, Human samples. Cited in 5 publications. Immunogen corresponding to Native Full Length Protein corresponding to Rabbit ALDOA.
Preservative: 0.01% Gentamicin sulphate
Constituents: 1% BSA, 0.88% Sodium chloride, 0.27% Tripotassium orthophosphate
IgG fraction antibody purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer.
Aldolase also known as fructose-bisphosphate aldolase is an enzyme that plays a critical role in glycolysis catalyzing the reversible cleavage of fructose 16-bisphosphate into glyceraldehyde-3-phosphate and dihydroxyacetone phosphate. Aldolase is a homotetramer with a molecular mass of approximately 158 kDa. It is highly expressed in liver muscle and brain tissues. Aldolase consists of three isoforms: aldolase A B and C each predominant in different tissues contributing to tissue-specific roles within the organism.
Aldolase catalyzes an important reaction in energy metabolism ensuring the continuation of glycolytic flux which is essential for ATP production. Aldolases do not form part of larger protein complexes. However they interact with other enzymes within the glycolytic pathway to facilitate a smooth metabolic flow. Moreover aldolase A plays an additional role in gluconeogenesis the pathway involved in synthesizing glucose from non-carbohydrate sources.
Aldolase is an essential part of glycolysis and gluconeogenesis pathways. In glycolysis it partners with enzymes like phosphofructokinase and enolase to breakdown glucose for energy production. During gluconeogenesis aldolase works with enzymes including fructose-16-bisphosphatase to create glucose vital for maintaining blood sugar levels during fasting. Through these pathways aldolase ensures balance between energy-producing and energy-consuming states within the cell.
Mutations or deficiencies in aldolase particularly aldolase A have been linked to glycogen storage disease type XII which results in muscle weakness and exercise intolerance. Aldolase B deficiency is known to cause hereditary fructose intolerance leading to liver and renal complications. These conditions highlight the importance of aldolase in maintaining metabolic health with implications for proteins within the same pathways potentially affecting their functions and expression levels.
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4-12% tris glycine gradient gel for SDS-PAGE
All lanes: Western blot - HRP Anti-Aldolase antibody (ab181662) at 1/1000 dilution
All lanes: A293 whole cell lysate
Developed using the ECL technique.
Predicted band size: 39 kDa
Immunoprecipitation and Western Blot analysis.
300 μl aliquots of whole anti-aldolase antiserum were used to precipitate varying amounts of purified aldolase and precipitates with controls were compared by SDS-PAGE and Western blot. Samples shown in the image are:
1. Purified aldolase
2. 300 μl antiserum with no antigen (negative control)
3. 300 μl antiserum with ~100 μl aldolase (2.5 mg/ml)
4. 300 μl antiserum with ~200 μl aldolase (2.5 mg/ml)
All lanes: Immunoprecipitation - HRP Anti-Aldolase antibody (ab181662)
Predicted band size: 39 kDa
Immunoprecipitation was performed with 300 μl of anti-Aldolase antiserum and an equal volume of varied amounts (diluted from a stock solution of ~2.5 mg/ml) of purified aldolase in PBS. Rabbit Adolase (from rabbit muscle) was used.
1. Purified Aldolase (1μg)
2. Precipitation negative control (antiserum + No antigen)
3. 300 μl antiserum + 20 μl Aldolase
4. 300 μl antiserum + 80 μl Aldolase
5. 300 μl antiserum + 120 μl Aldolase
6. 300 μl antiserum + 150 μl Aldolase
7. 300 μl antiserum + 300 μl Aldolase
All lanes: Immunoprecipitation - HRP Anti-Aldolase antibody (ab181662)
Predicted band size: 39 kDa
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