Votre recherche pour: 4-Keto-L-proline+hydrobromide

Fournisseur: TCI

Description: Propylamine hydrobromide ≥97.0% (par azote total et analyse par titration)

Fournisseur: TCI

Description: Ethylamine hydrobromide ≥98.0% (par azote total et analyse par titration)

Fournisseur: TCI

Description: N-Ethyl-1-naphthylamine hydrobromide ≥98.0% (par analyse titrimétrique)

Numéro de catalogue: (APOSOR470746-1G)

Fournisseur: Apollo Scientific

Description: 5-Bromo-N,N-diethyl-1-pentanamine hydrobromide

UOM: 1 * 1 g

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Numéro de catalogue: (APOSOR470748-1G)

Fournisseur: Apollo Scientific

Description: 4-Bromo-N,N-diethyl-1-butanamine hydrobromide

UOM: 1 * 1 g

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Fournisseur: TCI

Description: 4-Fluoroaniline hydrobromide ≥98.0% (par HPLC, analyse par titration)

Fournisseur: Thermo Fisher Scientific

Description: L-(-)-α-Amino-γ-butyrolactone hydrobromide 99%

MSMD

Numéro de catalogue: (BOSSBS-13453R-A488)

Fournisseur: Bioss

Description: GMD is a 372 amino acid protein that utilizes NADP as a cofactor to catalyze the conversion of GDP-mannose to GDP-4-keto-6-deoxymannose. GMD mutations are involved in resistance to TRAIL (tumor necrosis factor-related apoptosis-inducing ligand)-induced apoptosis. The gene encoding GMD maps to human chromosome 6, which contains 170 million base pairs and comprises nearly 6% of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease, Stickler syndrome and a susceptibility to bipolar disorder are all associated with genes that map to chromosome 6.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-11706R-A750)

Fournisseur: Bioss

Description: The aldo-keto reductase 7 (AKR7) family includes AKR7A2, AKR7A3 and AKR7A4 in human, AKR7A5 in mouse and AKR7A2 in rat, all of which function in the metabolism of aflatoxin B(1) and other dicarbonyl-containing compounds. More specifically, AKR7A proteins are involved in the metabolism of compounds with ketone groups on adjacent carbon atoms in a broad range of tissues, notably the liver. The human AKR7A2 gene maps to human chromosome 1p35-36, a region frequently deleted in sporadic colorectal cancer. The functional significance of this correlation lies in the constitutive expression of AKR7A2 in human liver to eliminate aflatoxin (an environmental carcinogen), thus acting as an endogenous chemo-preventative agent.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-11706R)

Fournisseur: Bioss

Description: The aldo-keto reductase 7 (AKR7) family includes AKR7A2, AKR7A3 and AKR7A4 in human, AKR7A5 in mouse and AKR7A2 in rat, all of which function in the metabolism of aflatoxin B(1) and other dicarbonyl-containing compounds. More specifically, AKR7A proteins are involved in the metabolism of compounds with ketone groups on adjacent carbon atoms in a broad range of tissues, notably the liver. The human AKR7A2 gene maps to human chromosome 1p35-36, a region frequently deleted in sporadic colorectal cancer. The functional significance of this correlation lies in the constitutive expression of AKR7A2 in human liver to eliminate aflatoxin (an environmental carcinogen), thus acting as an endogenous chemo-preventative agent.

UOM: 1 * 100 µl

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Fournisseur: Merck

Description: La gamme Aquastar™ comporte des réactifs pour le dosage de l'eau par titrage selon Karl Fischer, pour un large éventail de substrats et par toute une variété de méthodologies. Elle offre des réactifs à un ou deux composants, des reáctifs combinés pour la coulométrie, des solvants pour les huiles et les graisses, des réactifs et solvants pour le dosage de l'eau dans les cétones et les aldéhydes. Des étalons sont également disponibles.

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Numéro de catalogue: (TCIAP1666-25G)

Fournisseur: TCI

Description: Pyridine hydrobromide ≥98.0% (par HPLC, analyse par titration)

UOM: 1 * 25 g

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Fournisseur: TCI

Description: Butylamine hydrobromide ≥98.0% (par azote total et analyse par titration)

Fournisseur: TCI

Description: Dodecylamine hydrobromide ≥98.0% (par azote total et analyse par titration)

Numéro de catalogue: (BOSSBS-11401R-CY7)

Fournisseur: Bioss

Description: DD3 is a unique enzyme that can specifically catalyze the dehydrogenation of trans-benzenedihydrodiol and trans-naphthalenedihydrodiol.Human liver contains isoforms of dihydrodiol dehydrogenase (DD1, DD2, DD3 and DD4), which belong to the aldo-oxo reductase/aldo-keto reductase (AKR) superfamily, have 20Alpha- or 3Alpha-hydroxysteroid dehydrogenase (HSD) activity. DD1 is also designated AKR1C1, DDH or DDH1 while DD2 also can be designated AKR1C2, dDD, BABP or DDH2. AKR1C3 and 3Alpha-HSD are alternate designations for DD3, while DD4 also can be called AKR1C4, CD or CHDR. DD1 and DD2 are 20Alpha-HSDs, whereas DD3 and DD4 are the 3Alpha-HSDs. The multiple human cytosolic dihydrodiol dehydrogenases are involved in the metabolism of xenobiotics, such as polycyclic aromatic hydrocarbons, pesticides and steroid hormones, and are responsible for the reduction of ketone-containing drugs by using NADH or NADPH as a cofactor. The 20Alpha-HSD catalyzes the reaction of progesterone to the inactive form 20Alpha-hydroxyprogesterone. The 3Alpha-HSD is a cytosolic, monomeric, NADPH-dependent oxidoreductase that reduces 3-keto-5-dihydrosteroids to their tetrahydro products. DD1 and DD2 are ubiquitously expressed, whereas DD4 mRNA is restricted to the liver.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-11401R-FITC)

Fournisseur: Bioss

Description: DD3 is a unique enzyme that can specifically catalyze the dehydrogenation of trans-benzenedihydrodiol and trans-naphthalenedihydrodiol.Human liver contains isoforms of dihydrodiol dehydrogenase (DD1, DD2, DD3 and DD4), which belong to the aldo-oxo reductase/aldo-keto reductase (AKR) superfamily, have 20Alpha- or 3Alpha-hydroxysteroid dehydrogenase (HSD) activity. DD1 is also designated AKR1C1, DDH or DDH1 while DD2 also can be designated AKR1C2, dDD, BABP or DDH2. AKR1C3 and 3Alpha-HSD are alternate designations for DD3, while DD4 also can be called AKR1C4, CD or CHDR. DD1 and DD2 are 20Alpha-HSDs, whereas DD3 and DD4 are the 3Alpha-HSDs. The multiple human cytosolic dihydrodiol dehydrogenases are involved in the metabolism of xenobiotics, such as polycyclic aromatic hydrocarbons, pesticides and steroid hormones, and are responsible for the reduction of ketone-containing drugs by using NADH or NADPH as a cofactor. The 20Alpha-HSD catalyzes the reaction of progesterone to the inactive form 20Alpha-hydroxyprogesterone. The 3Alpha-HSD is a cytosolic, monomeric, NADPH-dependent oxidoreductase that reduces 3-keto-5-dihydrosteroids to their tetrahydro products. DD1 and DD2 are ubiquitously expressed, whereas DD4 mRNA is restricted to the liver.

UOM: 1 * 100 µl

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