This is a synthetic peptide designed for use in combination with anti-ALDOA antibody (Catalog #: ARP48130_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
ALDOA
Reactivité: Humain, Souris, Rat
Hôte: Synthetic
BP, BI
Indications d'application
Each Investigator should determine their own optimal working dilution for specific applications.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Concentration
1 mg/mL
Buffer
Final peptide concentration is 1 mg/mL in PBS.
Conseil sur la manipulation
Avoid repeated freeze-thaw cycles.
Stock
-20 °C
Stockage commentaire
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
Antigène
ALDOA
(Aldolase A, Fructose-Bisphosphate (ALDOA))
Synonymes
ALDA Peptide, GSD12 Peptide, aldoa Peptide, cb79 Peptide, sb:cb79 Peptide, wu:fa28b10 Peptide, wu:fb10b11 Peptide, ALDOA Peptide, Aldo-1 Peptide, Aldo1 Peptide, RNALDOG5 Peptide, hm:zeh0036 Peptide, zgc:77696 Peptide, aldolase, fructose-bisphosphate A Peptide, aldolase a, fructose-bisphosphate, a Peptide, aldolase, fructose-bisphosphate A S homeolog Peptide, aldolase A, fructose-bisphosphate Peptide, aldolase a, fructose-bisphosphate, b Peptide, ALDOA Peptide, aldoaa Peptide, aldoa Peptide, aldoa.S Peptide, Aldoa Peptide, aldoab Peptide
Sujet
ALDOA is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. 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.This gene product, 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 of this gene results in multiple transcript variants which encode the same protein.
Alias Symbols: ALDA, MGC10942, MGC17716, MGC17767, GSD12
Protein Interaction Partner: ALDOA,ATP6V1E1,DYNLL1,GPD2,MYOC,PLD2,SUMO4,TGM2,TUBB,XRN1,ATP6V1E1,FANCA,OSBPL10,PLD2,USP15,XRN1