You Searched For: 6-Bromochromone-2-carboxylic+acid


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Description: Synonym Hydrogen chloride solution, acc. to DIN 51558 part 1 c(HCl) = 0.1 mol/l (0,1 N) Titripur gade.
Catalog Number: CA1.00326.1000
Supplier: MilliporeSigma

Description: Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human , Gene ID: 4084 , Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-50 amino acids from the N-terminal region of human MXD1
Catalog Number: 89518-482
Supplier: Abgent


Description: Hydrochloric Acid, 10 g/L HCl, Cas number: 7647-01-0, 7732-18-5, Molecular Formula: HCl, H2O, Molecular weight: 36.46g/mol, 18.01g/mol, Appearance/Form: Colorless liquid, Size: 1L Poly natural
Catalog Number: RCR3563000-1A
Supplier: Ricca Chemical

Description: Sequence: Abz-Gly-OH · HCl
Catalog Number: E-2920.0005BA
Supplier: Bachem Americas


Description: Hydrochloric Acid, 37 Percent, NF is an excellent acidifying reagent. 
Catalog Number: 75811-374
Supplier: Spectrum Chemicals


Description: MDL: MFCD00011324
Catalog Number: CAAA35642-K2
Supplier: Thermo Scientific Chemicals

Description: TRC (R)-3-Aminopiperidine Dihydrochloride
Catalog Number: 77977-345
Supplier: LGC Standards

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Description: CAS Number: 2451-62-9
MDL Number: MFCD00080670
Molecular Formula: C12H15N3O6
Molecular Weight: 297.27
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 108
Flash Point (°C): 170
Catalog Number: TCI0428-100G
Supplier: TCI America

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: 10490-676
Supplier: Bioss


Description: Anti-SLAMF7 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Recombinant Protein, 23-227 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower
Catalog Number: 10094-688
Supplier: Proteintech


Description: Cell permeable non-tubulin-interacting mitosis inhibitor. Blocks mitosis (IC50=14µM) by binding to the mitotic kinesin Eg5.
Catalog Number: 89158-918
Supplier: Enzo Life Sciences


Description: Cs6
Catalog Number: CA1.09911.0001
Supplier: MilliporeSigma

Description: Hydrochloric acid, Purity:25%, Synonyms:Hydrogen chloride solution, Application:for analysis EMSURE
Catalog Number: CA1.00316.9025
Supplier: MilliporeSigma

Description: Naturally occuring antioxidant and inhibitor of lipoxygenase
Catalog Number: CAAAAL03149-03
Supplier: Thermo Scientific Chemicals

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: 10490-668
Supplier: Bioss


Description: (-)-Di-p-toluoyl-L-tartaric acid 98%
Catalog Number: CAAAB22972-22
Supplier: Thermo Scientific Chemicals

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