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Glycogen Catabolism

pathways : Glycogen Catabolism
pathways:

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Related Pathways to "Glycogen Catabolism" content :


Related Genes to "Glycogen Catabolism" content :

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Catalog number Product name Quantity
25-713 FAH is the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia. This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH de 0.05 mg
29-619 FAH is the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia.This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH def 0.1 mg
bs-2359R-Cy7 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, Cy7 Conjugated 100ul
bs-2359R-Cy5 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, Cy5 Conjugated 100ul
bs-2359R-Cy5.5 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, Cy5.5 Conjugated 100ul
bs-2359R-Cy3 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, Cy3 Conjugated 100ul
bs-2359R Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody 100ul
26-612 4-aminobutyrate aminotransferase (ABAT) is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic s 0.05 mg
bs-2359R-A555 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, ALEXA FLUOR 555 Conjugated 100ul
bs-2359R-A647 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, ALEXA FLUOR 647 Conjugated 100ul
E2GN-100 EnzyChrom™ Glycogen Assay Kit, Quantitative determination of glycogen by colorimetric (570nm) or fluorometric (585_530nm) methods 100Tests
bs-2359R-A350 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, ALEXA FLUOR 350 Conjugated 100ul
bs-2359R-A488 Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, ALEXA FLUOR 488 Conjugated 100ul
A024102 Rabbit Anti-Glycogen per Glycogen synthase 1 Ab 100ul
30-415 CT1 is a member of the 3-oxoacid CoA-transferase gene family. It is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversi 0.05 mg
26-067 HAL is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. HAL defects cause histidinemia which is characteriz 0.05 mg
30-098 HAL is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. HAL defects cause histidinemia which is characteriz 0.1 mg
30-414 OXCT1 is a member of the 3-oxoacid CoA-transferase gene family. It is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the rever 0.05 mg
X2206P Human Phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V) (PYGM) Antigen Immunoaffinity Purified Polyclonal 50
GWB-26C6F2 Phosphorylase Glycogen; Muscle (McArdle Syndrome Glycogen Storage Disease Type V) (PYGM) Rabbit anti-Human Polyclonal Antibody
E2GN-100 EnzyChrom™ Glycogen Assay Kit, Quantitative determination of glycogen by colorimetric (570nm) or fluorometric (585_530nm) methods. Procedure 30 min. Kit size 100 tests. Detection limit 2 µg_mL. She 100tests
bs-2359R-FITC Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, FITC Conjugated 100ul
bs-2359R-Biotin Rabbit Anti-Glycogen-Glycogen synthase 1 Polyclonal Antibody, Biotin Conjugated 100ul
29-607 PRODH2 is similar to proline dehydrogenase (oxidase) 1, a mitochondrial enzyme which catalyzes the first step in proline catabolism. The function of this protein has not been determined.The protein en 0.05 mg
29-593 HSD17B6 has both oxidoreductase and epimerase activities and is involved in androgen catabolism. The oxidoreductase activity can convert 3 alpha-adiol to dihydrotestosterone, while the epimerase activ 0.1 mg


 

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