Du søkte etter: 3-Carbamyl-1-methylpyridinium+chloride

Produsent: TCI

Beskrivelse: 3-Carbamyl-1-methylpyridinium chloride 98,0 HPLC, T

Produsent: TCI

Beskrivelse: 1-Butyl-4-methylpyridinium chloride 99,0 HPLC, T

Produsent: TCI

Beskrivelse: 1-Butyl-3-methylpyridinium chloride ≥98.0% (by HPLC, titration analysis)

Produsent: TCI

Beskrivelse: 1-Methylpyridinium chloride ≥98.0% (by titrimetric analysis)

Artikkenummer: (APOSOR938667-25G)

Produsent: Apollo Scientific

Beskrivelse: 1-Butyl-4-methylpyridinium chloride 98%

UOM: 1 * 25 g

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Artikkenummer: (335630-25G)

Produsent: SIGMA ALDRICH MICROSCOPY

Beskrivelse: Alcian Blue, pyridine variant, Dye content ≥85 % (Alcian Blue-tetrakis(methylpyridinium) chloride)

UOM: 1 * 25 g

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Artikkenummer: (TCIAH0967-5G)

Produsent: TCI

Beskrivelse: 1-Hexadecyl-4-methylpyridinium chloride hydrate ≥98.0% (by titrimetric analysis)

UOM: 1 * 5 g

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Artikkenummer: (APOSOR22249-500MG)

Produsent: Apollo Scientific

Beskrivelse: 1-(4-Methoxyphenyl)-3-(3-methylpyridinium-1-yl)prop-2-en-1-one chloride

UOM: 1 * 500 mg

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Artikkenummer: (APOSOR22250-500MG)

Produsent: Apollo Scientific

Beskrivelse: N-[(1E)-3-(4-Chlorophenyl)-3-oxoprop-1-en-1-yl]-3-methylpyridinium chloride

UOM: 1 * 500 mg

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Produsent: TCI

Beskrivelse: Amprolium Hydrochloride ≥98.0% (by HPLC, titration analysis) for biochemical research

Artikkenummer: (TCIAT1429-5G)

Produsent: TCI

Beskrivelse: Trigonelline hydrochloride ≥98.0% (by HPLC, titration analysis)

UOM: 1 * 5 g

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Artikkenummer: (TCIAM0819-25G)

Produsent: TCI

Beskrivelse: Pyridine-2-aldoxime methochloride ≥98.0% (by HPLC, titration analysis)

UOM: 1 * 25 g

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Produsent: Thermo Fisher Scientific

Beskrivelse: Pyridine-2-aldoxime methochloride 97

HMS

Produsent: MP Biomedicals

Beskrivelse: Applications:
Urea is used for the denaturation of proteins and as a mild solubilization agent for insoluble or denatured proteins. Useful for renaturing proteins from samples already denatured with 6 M guanidine chloride such as inclusion bodies and in the extraction of the mitochondrial complex. It is commonly used to solubilize and denature proteins for denaturing isoelectric focusing and two-dimensional electrophoresis and in acetic acid-urea PAGE gels. May be used with guanidine hydrochloride and dithiothreitrol (DTT) in the refolding of denatured proteins into their native or active form. Urea is used in cell or tissue culture media to increase the osmolality. Urea has also been used as fertilizer because of the easy availability of nitrogen; in animal feeds; it is reacted with aldehydes to make resins and plastics; condensed with malonic ester to form barbituric acid; used in the paper industry to soften cellulose.
Biochem/physiol Actions:
Urea has been shown to act as an aldosterone antagonist in the development of peanut agglutinin binding in cultured embryonic renal collecting duct epithelial cells. Urea is the principal end product of nitrogen metabolism in most mammals, formed by the enzymatic reactions of the Kreb's cycle.
Typical Working Concentration:
The use of 2 g/L urea in the culture of Kluyveromyces marxianus to produce a thermostable extracellular lipase has been described. Urea is typically used at a concentration of 8 M for protein denaturation or solubilization. A final concentration of 5 M urea is commonly used in molecular biology for sequencing gels. To prevent carbamylation, do not heat urea containing buffers above 37 °C

Produsent: TCI

Beskrivelse: 1-Ethyl-2-methylpyridinium bromide 98,0 HPLC, T

Artikkenummer: (BOSSBS-8287R)

Produsent: Bioss

Beskrivelse: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

UOM: 1 * 100 µl

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