You Searched For: Diisopropyl+fumarate


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Catalog Number: (75834-526)
Supplier: Restek
Description: Standard Diisopropyl ether (DIPE), CAS: 108-20-3, Concentration in Solvent: 2,000 ug/mL in P and T methanol, Shelf Life: 6 months, Storage: 0 degree C or colder, Volume: 1 mL/ampule.


Catalog Number: (10086-770)
Supplier: Proteintech
Description: FAH is also named as FAA(fumarylacetoacetase), the last enzyme in tyrosine degradation, functionally important in the liver and kidney. FAH is a metabolic enzyme catalyzing the last step of tyrosine and phenylalanine catabolism: the hydrolysis of fumarylacetoacetate into acetoacetate and fumarate. In humans, deficiency of this activity is associated with the metabolic disease hereditary tyrosinaemia type I, which is also known as hepatorenal tyrosinaemia.


Catalog Number: (75835-572)
Supplier: Restek
Description: The california oxygenates mix consists of five components they are tert-amyl methyl ether (TAME) 2000 μg/ml, tert-butanol (TBA) 10000 μg/ml, diisopropyl ether (DIPE) 2000 μg/ml, ethyl-tert-butyl ether (ETBE) 2000 μg/ml and methyl tert-butyl ether (MTBE) 2000 μg/ml.


Supplier: TCI America
Description: CAS Number: 61699-62-5
MDL Number: MFCD00075125
Molecular Formula: C10H14O4
Molecular Weight: 198.22
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 46
Flash Point (°C): 113
Catalog Number: (103011-122)
Supplier: Anaspec Inc
Description: Selectively binding to GC sequence.


Catalog Number: (10108-304)
Supplier: Prosci
Description: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.


Catalog Number: (10343-924)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Catalog Number: (10343-920)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Catalog Number: (10343-918)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Catalog Number: (76082-592)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Catalog Number: (76082-594)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Catalog Number: (10343-906)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Catalog Number: (10343-926)
Supplier: Bioss
Description: Gluconolactonase with low activity towards other sugar lactones, including gulonolactone and galactonolactone. Can also hydrolyze diisopropyl phosphorofluoridate and phenylacetate (in vitro). Calcium-binding protein. Modulates Ca(2+) signaling, and Ca(2+)-dependent cellular processes and enzyme activities (By similarity).


Supplier: Thermo Scientific Chemicals
Description: Liquid. Flammable. Corrosive.
Catalog Number: (10082-556)
Supplier: Proteintech
Description: ADSL(adenylosuccinate lyase) is also named as AMPS, ASase, ASL and belongs to the lyase 1 family. It is an enzyme involved in 2 pathways of purine nucleotide metabolism and catalyzes cleavage of succinyl groups to yield fumarate. Defects in ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency). In humans, mutations in ADSL lead to an inborn error of metabolism originally characterized by developmental delay, often with autistic features..The ADSL enzymatic activity is reduced in lymphocytes and red blood cells of the patient with severe psychomotor retardation. It has 2 isoforms produced by alternative splicing.


Supplier: TCI America
Description: CAS Number: 17536-00-4
MDL Number: MFCD00671516
Molecular Formula: C9H16N2
Molecular Weight: 152.24
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 88
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