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Catalog Number: (TCD0602-025G)
Supplier: TCI America
Description: CAS Number: 473-81-4
MDL Number: MFCD00065927
Molecular Formula: C3H6O4
Molecular Weight: 106.08
Form: Clear Liquid
Color: Colorless

Supplier: Ambeed
Description: 2,3-Dihydroxypropanoic acid, Purity: 20% in water, CAS Number: 473-81-4, Appearance: Liquid, Storage: Sealed in dry, Room Temperature, Size: 1G

Supplier: Thermo Scientific Chemicals
Description: DL-Glyceric acid calcium salt dihydrate. Grade:98, Melting Point ca 140*[degree]C. Boiling Point C:NA. C6H10CaO8. 2H2O. 67525-74-0.
Supplier: Spectrum Chemicals
Description: DL-Glyceraldehyde, purity: 90 %, CAS number: 56-82-6, Molecular Formula: C3H6O3, Molecular weight: 90.08, Form: Solid, synonyms: Glyceraldehyde, (+-)-, DL-Glyceric aldehyde, size: 5 g
Catalog Number: (10298-280)
Supplier: Bioss
Description: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.


Catalog Number: (10298-274)
Supplier: Bioss
Description: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.


Catalog Number: (10298-272)
Supplier: Bioss
Description: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.


Catalog Number: (10298-260)
Supplier: Bioss
Description: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.


Catalog Number: (10298-276)
Supplier: Bioss
Description: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.


Catalog Number: (10298-278)
Supplier: Bioss
Description: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.


Supplier: Matrix Scientific
Description: MF=C7H12O4 MW=160.17 CAS=52373-72-5 MDL=MFCD00066527 1G

Supplier: Ambeed
Description: Methyl (R)-(+)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 95%

Supplier: TCI America
Description: CAS Number: 52373-72-5
MDL Number: MFCD00066527
Molecular Formula: C7H12O4
Molecular Weight: 160.17
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 78
Flash Point (°C): 75
Specific Gravity (20/20): 1.11
Specific rotation [a]20/D: 11 deg (neat)

SDS

Catalog Number: (76070-106)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000


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: (103267-584)
Supplier: Novus Biologicals
Description: The GLYCTK Antibody from Novus Biologicals is a rabbit polyclonal antibody to GLYCTK. This antibody reacts with human, mouse. The GLYCTK Antibody has been validated for the following applications: Western Blot, Immunohistochemistry, Immunohistochemistry-Paraffin.


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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