You Searched For: N-(Phenylsulfonyl)glycine+Methyl+Ester


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Catalog Number: (10334-566)
Supplier: Bioss
Description: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine.


Catalog Number: (10334-588)
Supplier: Bioss
Description: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine.


Catalog Number: (76009-778)
Supplier: Prosci
Description: Glycine N-methyltransferase catalyzes the synthesis of N-methylglycine (sarcosine) from glycine using S-adenosylmethionine (AdoMet) as the methyl donor. GNMT acts as an enzyme to regulate the ratio of S-adenosylmethionine to S-adenosylhomocysteine (AdoHcy) and participates in the detoxification pathway in liver cells.


Catalog Number: (10334-584)
Supplier: Bioss
Description: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine.


Supplier: MP Biomedicals
Description: Tricine, a zwitterionic buffer, was first prepared by good for use as a buffer for chloroplast reactions. It is structurally similar to Tris, but is much less inhibitory at high concentrations. The name tricine comes from tris and glycine from which it was derived.

SDS

Supplier: Thermo Scientific Chemicals
Description: N-Benzylglycine ethyl ester 96%

Catalog Number: (76101-978)
Supplier: Bioss
Description: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine.


Catalog Number: (10334-578)
Supplier: Bioss
Description: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine.


Supplier: Ambeed
Description: N-Benzylglycine ethyl ester 96%

Supplier: TCI America
Description: CAS Number: 164462-16-2
Molecular Formula: C7H11NO6
Molecular Weight: 271.11
Purity/Analysis Method: >95.0% (T)
Form: Crystal
Color: White
Supplier: Ambeed
Description: Tert-butyl 2-((4-chlorobenzyl)((5-nitrothiophen-2-yl)methyl)amino)acetate, Purity: 98+%, CAS Number: 1216744-19-2, Appearance: Solid, Storage: Keep in dark place, Sealed in dry, 2-8 C, Size: 5mg

Catalog Number: (10334-580)
Supplier: Bioss
Description: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine.


Supplier: TCI America
Description: CAS Number: 922-32-7 MDL Number: MFCD00014351 Molecular Formula: C4H10N3O5P Molecular Weight: 255.08 Purity/Analysis Method: <gt/>98.0% (HPLC) Form: Crystal Storage Temperature: 0-10°C
Supplier: Spectrum Chemicals
Description: Guanidinoacetic Acid, also known 2-Guanidinoacetic acid, is a metabolite of glycine used as a supplement and a precursor of creatine.

SDS

Supplier: Spectrum Chemicals
Description: N-Lauroylsarcosine Sodium Salt, Appearance: Powder, Color: White, Cas number: 137-16-6, Molecular Weight: 293.39, Formula: C15H28NNaO3, Synonyms: Sodium N-lauroylsarcosinate, Sodium N-Dodecanoyl-N-methyl-glycinate, Sarcosyl, Sarkosyl NL, Size: 12 kg

SDS

Supplier: Anaspec Inc
Description: This peptide is Histone H3 amino acid residues 21 to 44 di-methylated at Lys-27 with an additional C-terminal glycine followed by a biotinylated lysine. Provided at >95% peptide purity, this peptide was dissolved in distilled water at 1 mg/ml and re-lyophilized to powder form.
Sequence:ATKAAR-K(Me2)-SAPATGGVKKPHRYRPG-GK(Biotin)
MW:2945.5 Da
% peak area by HPLC:95
Storage condition:-20° C

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