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Proteintech
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Immunogen sequence: MAHRFPALT QEQKKELSEI AQSIVANGKG ILAADESVGT MGNRLQRIKV ENTEENRRQF REILFSVDSS INQSIGGVIL FHETLYQKDS QGKLFRNILK EKGIVVGIKL DQGGAPLAGT NKETTIQGLD GLSERCAQYK KDGVDFGKWR AVLRIADQCP SSLPIQENAN ALARYASICQ QNGLVPIVEP EVIPDGDHDL EHCQYVTEKV LAAVYKALND HHVYLEGTLL KPNMVTAGHA CTKKYTPEQV AMATVTALHR TVPAAVPGIC FLSGGMSEED ATLNLNAINL CPLPKPWKLS FSGVARLQTR RQPRRLL (1-316 aa encoded by BC029399)
Fructose-1,6-bisphosphate aldolase is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related 'housekeeping' genes exhibiting developmentally regulated expression of the different isozymes. The developing embryo produces aldolase A, which is produced in even greater amounts in adult muscle where it can be as much as 5% of total cellular protein. In adult liver, kidney and intestine, aldolase A expression is repressed and aldolase B is produced. In brain and other nervous tissue, aldolase A and C are expressed about equally. There is a high degree of homology between aldolase A and C. Defects in ALDOB cause hereditary fructose intolerance.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Aldolase 2; aldolase 2, B isoform; Aldolase B fructose-biphosphate; Aldolase B, fructose-biphosphate; aldolase B, fructose-bisphosphatase; aldolase B, fructose-bisphosphate; Fructose-bisphosphate aldolase B; Liver-type aldolase
Gene Aliases: ALDB; Aldo-2; ALDO2; ALDOB; BC016435; LIV10
UniProt ID: (Human) P05062, (Mouse) Q91Y97
Entrez Gene ID: (Human) 229, (Mouse) 230163, (Rat) 24190
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