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Hai cercato: Hydrogen+peroxide-urea


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Codice catalogo: (BOSSBS-9515R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-CY7
Codice articolo locale: BOSSBS-9515R-CY7
Descrizione: Catalyzes the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous signaling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure.Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2060R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-2060R-A350
Codice articolo locale: BOSSBS-2060R-A350
Descrizione: Forms a channel with a broad specificity. Mediates passage of a wide variety of non-charged solutes including carbamides, polyols, purines, and pyrimidines in a phloretin- and mercury-sensitive manner, whereas amino acids, cyclic sugars, Na(+), K(+), Cl(-), and deprotonated monocarboxylates are excluded. Also permeable to urea and glycerol.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-A680
Codice articolo locale: BOSSBS-9515R-A680
Descrizione: catalyses the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous Signalling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure. Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterised by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-CY3
Codice articolo locale: BOSSBS-9515R-CY3
Descrizione: Catalyzes the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous signaling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure.Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-FITC
Codice articolo locale: BOSSBS-9515R-FITC
Descrizione: Catalyzes the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous signaling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure.Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (PRSI91-986)
Fornitore: ProSci Inc.
Codice articolo fornitore: 91-986
Codice articolo locale: PRSI91-986
Descrizione: Argininosuccinate Synthase (ASS1) is an urea cycle enzyme with a tetrameric structure composed of identical subunits. ASS1 is involved in the synthesis of arginine and catalyses that condensation of citrulline and aspartate to argininosuccinate using ATP. ASS1 is important to the urea cycle as it catalyses the important second last step in the arginine biosynthetic pathway. ASS1 mainly expressed in periportal hepatocytes, but also in most other body tissues. A deficiency of ASS1 causes citrullinemia (CTLN1), an autosomal recessive disease which is characterised by severe vomiting spells and mental retardation.
UOM: 1 * 50 µG


Codice catalogo: (30015.)
Fornitore: Biotium
Codice articolo fornitore: 30015
Codice articolo locale: BTIU30015
Descrizione: DAB (3,3′-diaminobenzidine) reacts with HRP in the presence of peroxide to yield an insoluble brown-colored product at locations where peroxidase-conjugated antibodies are bound to samples. The brown precipitate is insoluble in alcohol and other organic solvents, making it an excellent substrate for immunohistochemical staining that requires the use of traditional counterstains and mounting media.
UOM: 1 * 1 KIT


Codice catalogo: (BOSSBS-2060R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-2060R-HRP
Codice articolo locale: BOSSBS-2060R-HRP
Descrizione: Forms a channel with a broad specificity. Mediates passage of a wide variety of non-charged solutes including carbamides, polyols, purines, and pyrimidines in a phloretin- and mercury-sensitive manner, whereas amino acids, cyclic sugars, Na(+), K(+), Cl(-), and deprotonated monocarboxylates are excluded. Also permeable to urea and glycerol.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2060R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-2060R-FITC
Codice articolo locale: BOSSBS-2060R-FITC
Descrizione: Forms a channel with a broad specificity. Mediates passage of a wide variety of non-charged solutes including carbamides, polyols, purines, and pyrimidines in a phloretin- and mercury-sensitive manner, whereas amino acids, cyclic sugars, Na(+), K(+), Cl(-), and deprotonated monocarboxylates are excluded. Also permeable to urea and glycerol.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-A488
Codice articolo locale: BOSSBS-9515R-A488
Descrizione: Catalyzes the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous signaling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure.Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-A555
Codice articolo locale: BOSSBS-9515R-A555
Descrizione: Catalyzes the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous signaling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure.Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R-A750
Codice articolo locale: BOSSBS-9515R-A750
Descrizione: catalyses the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous Signalling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure. Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterised by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2060R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-2060R-CY7
Codice articolo locale: BOSSBS-2060R-CY7
Descrizione: Forms a channel with a broad specificity. Mediates passage of a wide variety of non-charged solutes including carbamides, polyols, purines, and pyrimidines in a phloretin- and mercury-sensitive manner, whereas amino acids, cyclic sugars, Na(+), K(+), Cl(-), and deprotonated monocarboxylates are excluded. Also permeable to urea and glycerol.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-9515R)
Fornitore: Bioss
Codice articolo fornitore: BS-9515R
Codice articolo locale: BOSSBS-9515R
Descrizione: Catalyzes the last step in the transsulfuration pathway from methionine to cysteine. Has broad substrate specificity. Converts cystathionine to cysteine, ammonia and 2-oxobutanoate. Converts two cysteine molecules to lanthionine and hydrogen sulfide. Can also accept homocysteine as substrate. Specificity depends on the levels of the endogenous substrates. Generates the endogenous signaling molecule hydrogen sulfide (H2S), and so contributes to the regulation of blood pressure.Defects in CTH are the cause of cystathioninuria (CSTNU). It is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine, leading to increased urinary excretion.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2060R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-2060R-CY3
Codice articolo locale: BOSSBS-2060R-CY3
Descrizione: Forms a channel with a broad specificity. Mediates passage of a wide variety of non-charged solutes including carbamides, polyols, purines, and pyrimidines in a phloretin- and mercury-sensitive manner, whereas amino acids, cyclic sugars, Na(+), K(+), Cl(-), and deprotonated monocarboxylates are excluded. Also permeable to urea and glycerol.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-2060R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-2060R-CY5.5
Codice articolo locale: BOSSBS-2060R-CY5.5
Descrizione: Forms a channel with a broad specificity. Mediates passage of a wide variety of non-charged solutes including carbamides, polyols, purines, and pyrimidines in a phloretin- and mercury-sensitive manner, whereas amino acids, cyclic sugars, Na(+), K(+), Cl(-), and deprotonated monocarboxylates are excluded. Also permeable to urea and glycerol.
UOM: 1 * 100 µl


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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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