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BPGM Protein, Human, Recombinant (His)

(Synonyms: DPGM, BPGM, BPG-Dependent PGAM, Bisphosphoglycerate Mutase, 3-Diphosphoglycerate Mutase, 3-Bisphosphoglycerate Synthase, 3-Bisphosphoglycerate Mutase Erythrocyte, 2) Copy Product Info

Synonyms: DPGM, BPGM, BPG-Dependent PGAM, Bisphosphoglycerate Mutase, 3-Diphosphoglycerate Mutase, 3-Bisphosphoglycerate Synthase, 3-Bisphosphoglycerate Mutase Erythrocyte, 2

Catalog No. TMPJ-00800 Copy Product Info
Bisphosphoglycerate Mutase (BPGM) is a member of the Phosphoglycerate Mutase family and BPG-Dependent PGAM subfamily. BPGM is a multifunctional enzyme. BPGM catalyzes 2,3-DPG synthesis via its synthetase activity, and 2,3-DPG degradation via its phosphatase activity. It also has phosphoglycerate phosphomutase activity. BPGM plays a major role in regulating hemoglobin oxygen affinity by controlling the levels of 2,3-bisphosphoglycerate (2,3-BPG). Deficiency of BPGM increases the affinity of cells for oxygen and result in hemolytic anemia.
BPGM Protein, Human, Recombinant (His)
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Pack SizePriceUSA StockGlobal StockQuantity
10 µg$11635 days35 days
20 µg$18635 days35 days
50 µg$35235 days35 days
100 µg$58235 days35 days
200 µg$96735 days35 days
500 µg$1,90035 days35 days
1 mg$2,73035 days35 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Bioactivity
Activity has not been tested. It is theoretically active, but we cannot guarantee it. If you require protein activity, we recommend choosing the eukaryotic expression version first.
Description
Bisphosphoglycerate Mutase (BPGM) is a member of the Phosphoglycerate Mutase family and BPG-Dependent PGAM subfamily. BPGM is a multifunctional enzyme. BPGM catalyzes 2,3-DPG synthesis via its synthetase activity, and 2,3-DPG degradation via its phosphatase activity. It also has phosphoglycerate phosphomutase activity. BPGM plays a major role in regulating hemoglobin oxygen affinity by controlling the levels of 2,3-bisphosphoglycerate (2,3-BPG). Deficiency of BPGM increases the affinity of cells for oxygen and result in hemolytic anemia.
Species
Human
Expression System
E. coli
TagC-6xHis
Accession NumberP07738
Amino AcidSer2-Lys259
ConstructionSer2-Lys259
Endotoxin< 0.1 ng/µg (1 EU/µg) as determined by LAL test.
FormulationSupplied as a 0.2 μm filtered solution of 20 mM Tris-HCl, 1 mM DTT, pH 8.0.
SynonymsDPGM, BPGM, BPG-Dependent PGAM, Bisphosphoglycerate Mutase, 3-Diphosphoglycerate Mutase, 3-Bisphosphoglycerate Synthase, 3-Bisphosphoglycerate Mutase Erythrocyte, 2
Research Background
Bisphosphoglycerate Mutase (BPGM) is a member of the Phosphoglycerate Mutase family and BPG-Dependent PGAM subfamily. BPGM is a multifunctional enzyme. BPGM catalyzes 2,3-DPG synthesis via its synthetase activity, and 2,3-DPG degradation via its phosphatase activity. It also has phosphoglycerate phosphomutase activity. BPGM plays a major role in regulating hemoglobin oxygen affinity by controlling the levels of 2,3-bisphosphoglycerate (2,3-BPG). Deficiency of BPGM increases the affinity of cells for oxygen and result in hemolytic anemia.
Chemical Properties
Molecular Weight30 KDa (reducing condition)
Storage & Solubility Information
ShippingProteins are shipped with blue ice.
StorageLyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.

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Related Tags: BPGM Protein, Human, Recombinant (His) chemical structure | BPGM Protein, Human, Recombinant (His) molecular weight