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Hľadali ste: DL-Methionine+sulphoxide


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Dodávateľ: BIORBYT
Opis: Anti-Methionine adenosyltransferase Rabbit Polyclonal Antibody

Katalógové číslo: (39496-100MG)
Dodávateľ: Merck
Opis: Organic Standard, ʟ-Methionine
Merná jednotka: 1 * 100 mg


Katalógové číslo: (50272-5ML-F)
Dodávateľ: Merck
Opis: Organic Standard, ʟ-Methionine hydrochloride solution
Merná jednotka: 1 * 5 mL


Katalógové číslo: (91016-100MG)
Dodávateľ: Merck
Opis: Organic Standard, ʟ-Methionine sulfoximine
Merná jednotka: 1 * 100 mg

Certifikáty


Dodávateľ: Merck
Opis: Accurate analytic results in UV/Vis and infrared spectroscopy depend on the use of very pure solvents for sample preparation. The Uvasol® solvents range has been specially designed for spectroscopy and other applications requiring solvents of the highest spectral purity. The refinement process allows a greater degree of security in applications and avoids misinterpretation of analytical results caused by traces of UV, IR and fluorescence contamination. Uvasol® solvents offer best UV transmittance. In all specifications the minimum transmittance for five typical wavelengths are identified. Furthermore the transmittance is specified in accordance with Reag. Ph. Eur. and ACS.
Katalógové číslo: (ANTIA11905-100)
Dodávateľ: ANTIBODIES.COM
Opis: Rabbit polyclonal antibody to Methionine Aminopeptidase 2 / p67 for WB with samples derived from human and mouse.
Merná jednotka: 1 * 100 µl

New Product


Katalógové číslo: (BIRBORB9208-100)
Dodávateľ: BIORBYT
Opis: Anti-Methionine adenosyltransferase Rabbit Polyclonal Antibody (FITC (Fluorescein))
Merná jednotka: 1 * 100 µG


Katalógové číslo: (PRSI29-561)
Dodávateľ: PROSCI
Opis: MAT1A catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.
Merná jednotka: 1 * 100 µG


Katalógové číslo: (PRSI27-079)
Dodávateľ: PROSCI
Opis: MAT2B belongs to the methionine adenosyltransferase (MAT) family. MAT catalyzes the biosynthesis of S-adenosylmethionine from methionine and ATP. This protein is the regulatory beta subunit of MAT.The protein encoded by this gene belongs to the methionine adenosyltransferase (MAT) family. MAT catalyzes the biosynthesis of S-adenosylmethionine from methionine and ATP. This protein is the regulatory beta subunit of MAT. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified.
Merná jednotka: 1 * 50 µG


Katalógové číslo: (PRSI55-674)
Dodávateľ: PROSCI
Opis: May have S-adenosyl-L-methionine-dependent methyl-transferase activity (Potential).
Merná jednotka: 1 * 400 µl

New Product


Katalógové číslo: (PRSI55-760)
Dodávateľ: PROSCI
Opis: May have S-adenosyl-L-methionine-dependent methyl-transferase activity (Potential).
Merná jednotka: 1 * 400 µl

New Product


Katalógové číslo: (PRSI56-593)
Dodávateľ: PROSCI
Opis: This gene catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. The encoded protein is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in this gene are associated with methionine adenosyltransferase deficiency.
Merná jednotka: 1 * 400 µl

New Product


Katalógové číslo: (ICNA091641454)
Dodávateľ: MP BIOMEDICALS
Opis: Minimum Essential Medium Eagle With Earle's Salts and 2,0 g/L sodium bicarbonate Without L-glutamine, L-cysteine, L-cystine, and L-methionine is generally used to grow attached cell lines, such as fibroblasts, in the presence of FBS, calf or horse sera.
Merná jednotka: 1 * 500 mL

Certifikáty


Katalógové číslo: (PRSI29-562)
Dodávateľ: PROSCI
Opis: MAT1A catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. MAT1A is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in its gene are associated with methionine adenosyltransferase deficiency.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.
Merná jednotka: 1 * 100 µG


Katalógové číslo: (PRSI55-466)
Dodávateľ: PROSCI
Opis: The N-terminal methionine excision pathway is an essential process in which the N-terminal methionine is removed from many proteins, thus facilitating subsequent protein modification. In mitochondria, enzymes that catalyze this reaction are celled methionine aminopeptidases (MetAps, or MAPs; EC 3.4.11.18) (Serero et al., 2003 [PubMed 14532271]).
Merná jednotka: 1 * 400 µl

New Product


Katalógové číslo: (PRSI29-728)
Dodávateľ: PROSCI
Opis: N-methylation is one method by which drug and other xenobiotic compounds are metabolized by the liver. NNMT responsible for this enzymatic activity which uses S-adenosyl methionine as the methyl donor.N-methylation is one method by which drug and other xenobiotic compounds are metabolized by the liver. This gene encodes the protein responsible for this enzymatic activity which uses S-adenosyl methionine as the methyl donor.
Merná jednotka: 1 * 100 µG


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