Aldolase A, Fructose-Bisphosphate (ALDOA) (C-Term) Peptid
ALDOA
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle ALDOA Produkte
- ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
- Protein Region
- C-Term
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Sequenz
- ALQASALKAW GGKKENLKAA QEEYVKRALA NSLACQGKYT PSGQAGAAAS
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-ALDOA Antibody. 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.
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- Applikationshinweise
- Optimal working dilution should be determined by the investigator.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
- Hintergrund
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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.
Alias Symbols: ALDOA,ALDA,
Protein Size: 364 - Gen-ID
- 226
- NCBI Accession
- NP_908932
- UniProt
- P04075
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