Human Fructose-Bisphosphate Aldolase A (ALDOA) Protein

Este producto es parte de ALDOA - Fructose-Bisphosphate Aldolase A
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234€ (5 µg)

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935106861
info@markelab.com
name
Human Fructose-Bisphosphate Aldolase A (ALDOA) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx073104
tested applications
SDS-PAGE

Description

Human Aldolase-A is a recombinant protein expressed in E. coli.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
Fructose-Bisphosphate Aldolase A (ALDOA)
Host
E. coli
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Origin
Human
Observed MW
Molecular Weight: 41.5 kDa
Concentration: 1 mg/ml
Sequence Fragment: 1-364 AA.
Tag: N-terminal His tag
Expression
Recombinant
Purity
> 95% (SDS-PAGE)
Purification
Purified by proprietary chromatographic techniques.
Size 1
5 µg
Size 2
20 µg
Size 3
1 mg
Form
Liquid 
Tested Applications
SDS-PAGE
Buffer
20 mM Tris-HCl buffer, pH 8.0, containing 0.1 M NaCl and 10% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Store at 4 °C if the entire vial will be used within 4 weeks. Store at -20 °C for long term storage. For long term storage, it is recommended to add a carrier protein (0.1% HSA or BSA). Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P04075
Gene ID
226
OMIM
103850
Alias
ALDOA,ALDA
Background
Protein ALDOA
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

ALDOA is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate into glyceraldehyde-3-phosphate and dihydroxyacetone phosphate during glycolysis. It is widely expressed, particularly in muscle tissues and the brain, where it plays a crucial role in energy metabolism and ATP production. ALDOA is vital for providing energy to rapidly proliferating cells and tissues with high metabolic demands. Dysregulation of ALDOA has been associated with cancer progression, as elevated glycolytic activity (Warburg effect) fuels tumor growth. Mutations in ALDOA cause glycogen storage disease type XII, characterized by hemolytic anemia and muscle weakness due to impaired glycolytic flux. Its role in energy metabolism underscores its importance in cellular homeostasis, growth, and disease.

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ALDOA Antibody is a Rabbit Polyclonal antibody against ALDOA. The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.

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