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Catalog Number: (TCC1477-5G)
Supplier: TCI America
Description: CAS Number: 2312-23-4
MDL Number: MFCD00012935
Molecular Formula: C6H7ClN2
Molecular Weight: 179.04
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

Catalog Number: (10490-678)
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.


Supplier: TCI America
Description: 2,6-Dibromobenzaldehyde, Purity: >98.0%(GC), CAS Number: 67713-23-9, Molecular Formula: C7H4Br2O, Molecular Weight: 263.92, Form: Crystal-Powder, Solid, Color: Very pale yellow - Yellow, Size: 1G

SDS

Catalog Number: (89357-724)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to IDO1 (indoleamine 2,3-dioxygenase 1)


Catalog Number: (76110-738)
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: (TCP0491-500ML)
Supplier: TCI America
Description: CAS Number: 71-23-8
MDL Number: MFCD00002941
Molecular Formula: C3H8O
Molecular Weight: 60.10
Purity/Analysis Method: >99.5% (GC)
Form: Clear Liquid
Boiling point (°C): 97
Melting point (°C): -127
Flash Point (°C): 25
Specific Gravity (20/20): 0.80

Catalog Number: (CAAAA14988-06)
Supplier: Thermo Scientific Chemicals
Description: 5-Iodoisatin 97%

Catalog Number: (77980-632)
Supplier: LGC Standards
Description: TRC (2Alpha,3Beta)-2,3-Dihydroxy-urs-12-en-28-oic Acid

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Catalog Number: (10490-672)
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: (89296-136)
Supplier: Genetex
Description: Goat polyclonal antibody to Cystatin 8 (aa 23-34)


Supplier: Thermo Scientific Chemicals
Description: Pure Al<sub>2</sub>O<sub>3 </sub>Aluminium oxide, AL 23.

Catalog Number: (103888-682)
Supplier: ACROBIOSYSTEMS INC MS
Description: Mouse CD3 epsilon&CD3 gamma Heterodimer Protein, Fc, His Tag&Fc, Flag Tag (MALS verified), Source: expressed from HEK293, Predicted N-terminus: Asp 23 (CD3E) & Gln 23 (CD3G), Molecular weight: 41.5 kDa (CD3E) and 41.6 kDa (CD3G), Synonyms: CD3 epsilon & CD3 gamma, CD3E & CD3G, Size: 100uG


Catalog Number: (470010-846)
Supplier: Ward's Science
Description: Visually see the difference between Groups and Periods.

SDS


Catalog Number: (77179-598)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/6406] antibody to FGF 23 for IHC-P with samples derived from Human.


Catalog Number: (77179-590)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [FGF23/4579] antibody to FGF 23 for IHC-P with samples derived from Human.


Supplier: Biolegend
Description: Pacific Blue™ anti-mouse CD40 [3/23]; Isotype: Rat IgG2a, κ; Reactivity: Mouse; Apps: FC; Size: 100 μg

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