You Searched For: N-Fmoc-glycine

Catalog Number: (BJ33552-1L)

Supplier: Honeywell Research Chemicals

Description: Buffer solution, pH 13.0 (20 deg C), Glycine / sodium hydroxide / sodium chloride solution, color: colourless, Form: liquid, Container type: Poly Bottle, Size: 1L

SDS

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.

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: Thermo Scientific Chemicals

Description: Liquid

Certificates

Supplier: TCI America

Description: Dansylglycine [for Albumin binding assay], Purity: >98.0%(T), CAS Number: 1091-85-6, Molecular Formula: C14H16N2O4S, Molecular Weight: 308.35, Synonyms: N-[5-(Dimethylamino)naphthalene-1-sulfonyl]glycine, Dns-Gly-OH, Size: 25MG

Catalog Number: (CAAAH59967-03)

Supplier: Thermo Scientific Chemicals

Certificates

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: Honeywell Research Chemicals

Description: Nitrilotriacetic acid, Purity: >/=99% For complexometry, CAS Number: 139-13-9, Molecular Formula: N(CH2COOH)3, Molecular weight: 191.14 g/mol, Synonyms: N,N-Bis(carboxymethyl)glycine; NTA; Tris(carboxymethyl)amine, Size: 25KG

SDS

Catalog Number: (76101-980)

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: (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: (CA11027-624)

Supplier: Hach

Description: Monitor ClO2 levels on-site with the NEW Chlorine Dioxide Test Kit. The Chlorine Dioxide Test Kit uses the reliable and EPA-accepted DPD method to monitor ClO2 concentration, while eliminating chlorine interference through the addition of glycine. With 100 tests per kit and available range of 0-2 mg/L and resolution of 0.1 mg/L, operators can accurately monitor around the 0.8 mg/L regulated limit.

SDS

Catalog Number: (E-1965.0025BA)

Supplier: Bachem Americas

Description: Also known as Cyclo(-Gly-Gly), dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Supplier: TCI America

Description: CAS Number: 154445-77-9
MDL Number: MFCD00235804
Molecular Formula: C34H40N4O7S
Molecular Weight: 648.78
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -6 deg (C=1, DMF)
Storage Temperature: <0°C

SDS Certificates

Supplier: Bachem Americas

Description: Sieber amide resin has been developed for the Fmoc-SPPS of fully t-butyl protected peptide amides. Cleavage can be achieved with 1% TFA in methylene chloride. Scavengers may be required. As N-methylation increases the acid-lability of the peptide bond, Malakoutikhah et al. employed Sieber resin for obtaining short peptide amides containing multiple MePhe residues.

Supplier: MilliporeSigma

SDS

Catalog Number: (77438-244)

Supplier: Bioss

Description: Interconversion of serine and glycine.