Fructose-Bisphosphate Aldolase A (ALDOA) Peptide

Este producto es parte de ALDOA - Fructose-Bisphosphate Aldolase A
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175.5€ (100 µg)

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935106861
info@markelab.com
name
Fructose-Bisphosphate Aldolase A (ALDOA) Peptide
category
Proteins and Peptides
provider
Abbexa
reference
abx617181
tested applications
P-ELISA

Description

Fructose-Bisphosphate Aldolase A (ALDOA) Peptide is a synthetic peptide. 

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Immunogen Target
Fructose-Bisphosphate Aldolase A (ALDOA)
Host
Synthetic
Recommended Dilution
BL (predicted): 0.5 mg/ml. Optimal dilutions/concentrations should be determined by the end user.
Conjugation
Unconjugated
Observed MW
Sequence Fragment: Internal region (near N-Terminus): NSLACQGKYTPSGQ
Size 1
100 µg
Form
Lyophilized Reconstitute in deionized water.
Tested Applications
P-ELISA
Buffer
Prior to lyophilization: Deionized water.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P04075
Gene ID
226, 11674, 24189
NCBI Accession
NP_000025.1, NP_001230106.1
OMIM
103850
Alias
ALDOA,ALDA
Background
Protein ALDOA
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

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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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