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Catalog Number: (77176-836)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/6407] antibody to FGF 23 for IHC-P with samples derived from Human.


Catalog Number: (76110-740)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease: Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD). A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Catalog Number: (TCD3946-1G)
Supplier: TCI America
Description: CAS Number: 200880-40-6
MDL Number: MFCD00056649
Molecular Formula: C34H67O10P
Molecular Weight: 688.86
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 195
Storage Temperature: <0°C

Supplier: VWR International
Description: Hydrochloric acid 6.0 N, StandARd® volumetric solution, Macron Fine Chemicals™
Catalog Number: (77987-754)
Supplier: LGC Standards
Description: TRC 2,3-Thioepoxy Madol (1.0 mg/ml in Acetonitrile)

New Product


Catalog Number: (77994-307)
Supplier: LGC Standards
Description: TRC L-Threonine-2,3-d2

New Product


Supplier: TCI America
Description: CAS Number: 70728-23-3
MDL Number: MFCD02093461
Molecular Formula: C8H8O7
Molecular Weight: 216.15
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 134
Specific rotation [a]20/D: -96 deg (C=0.5, CHCl3)
Storage Temperature: <0°C

SDS

Supplier: TCI America
Description: CAS Number: 2065-23-8
MDL Number: MFCD00010227
Molecular Formula: C9H10O3
Molecular Weight: 166.18
Purity/Analysis Method: >99.0% (GC)
Form: Clear Liquid
Boiling point (°C): 245
Flash Point (°C): 111
Specific Gravity (20/20): 1.15
Supplier: TCI America
Description: [Protecting Reagent for Active Methylene]
CAS Number: 2225-23-2
MDL Number: MFCD00008550
Molecular Formula: C16H18O4S4
Molecular Weight: 402.56
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 74

SDS

Catalog Number: (77176-834)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/4580] antibody to FGF 23 for IHC-P with samples derived from Human.


Catalog Number: (77176-828)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/6404] antibody to FGF 23 for IHC-P with samples derived from Human.


Catalog Number: (77179-594)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/6372] antibody to FGF 23 for IHC-P with samples derived from Human.


Catalog Number: (77176-830)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/6406] antibody to FGF 23 for IHC-P with samples derived from Human.


Catalog Number: (10490-668)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Catalog Number: (ABCA_AB186337-100U)
Supplier: Abcam
Description: HRP Mouse monoclonal [N152B/23] to VDAC1/Porin.

New Product


Supplier: Biolegend
Description: Purified anti-mouse IL-12/IL-23 p40 [C15.6]; Isotype: Rat IgG1, κ; Reactivity: Mouse, IL-12/IL-23 p40 subunit (monomer, homodimer and heterodimer IL-12 p35/p40 or IL-23 p19/p40); Apps: ELISA Capture, IHC, IP, WB; Size: 500 μg

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