Hai cercato: S-(Carboxymethyl)-L-cysteine

Codice catalogo: (TCIAC0863-25G)

Fornitore: TCI

Codice articolo fornitore: C0863-25G

Codice articolo locale: TCIAC0863-25G

Descrizione: S-(Carboxymethyl)-L-cysteine ≥98.0% (by HPLC, titration analysis)

UOM: 1 * 25 g

Promo

Fornitore: Thermo Fisher Scientific

Descrizione: CAS No.: 638-23-3

MSDS Certificati

Fornitore: Thermo Fisher Scientific

Descrizione: S-(Carboxymethyl)-L-cysteine 97%

MSDS

Codice catalogo: (APOSOR9955T-10MG)

Fornitore: Apollo Scientific

Codice articolo fornitore: OR9955T-10MG

Codice articolo locale: APOSOR9955T-10MG

Descrizione: L-Cysteine-glutathione disulphide

UOM: 1 * 10 mg

Promo

Fornitore: Spectrum Chemical

Descrizione: S-Carboxymethyl-L-cysteine, also known as Rhinathiol or Humex, is a mucolytic that minimizes the viscosity of sputum so it can be used to treat chronic obstructive pulmonary disorder and bronchiectasis.

Codice catalogo: (PRSI26-882)

Fornitore: ProSci Inc.

Codice articolo fornitore: 26-882

Codice articolo locale: PRSI26-882

Descrizione: Several proteins have been found to be prenylated and methylated at their carboxyl-terminal ends. Prenylation was initially believed to be important only for membrane attachment. However, another role for prenylation appears to be its importance in protein-protein interactions. The only nuclear proteins known to be prenylated in mammalian cells are prelamin A- and B-type lamins. Prelamin A is farnesylated and carboxymethylated on the cysteine residue of a carboxyl-terminal CaaX motif. This post-translationally modified cysteine residue is removed from prelamin A when it is endoproteolytically processed into mature lamin A. NARF binds to the prenylated prelamin A carboxyl-terminal tail domain. It may be a component of a prelamin A endoprotease complex. NARF is located in the nucleus, where it partially colocalizes with the nuclear lamina. It shares limited sequence similarity with iron-only bacterial hydrogenases.Several proteins have been found to be prenylated and methylated at their carboxyl-terminal ends. Prenylation was initially believed to be important only for membrane attachment. However, another role for prenylation appears to be its importance in protein-protein interactions. The only nuclear proteins known to be prenylated in mammalian cells are prelamin A- and B-type lamins. Prelamin A is farnesylated and carboxymethylated on the cysteine residue of a carboxyl-terminal CaaX motif. This post-translationally modified cysteine residue is removed from prelamin A when it is endoproteolytically processed into mature lamin A. The protein encoded by this gene binds to the prenylated prelamin A carboxyl-terminal tail domain. It may be a component of a prelamin A endoprotease complex. The encoded protein is located in the nucleus, where it partially colocalizes with the nuclear lamina. It shares limited sequence similarity with iron-only bacterial hydrogenases. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene, including one with a novel exon that is generated by RNA editing.

UOM: 1 * 50 µG

Promo

Fornitore: MP Biomedicals

Descrizione: Storage: Store at +4 °C, store under nitrogen
Glutathione is the major low molecular weight thiol compound of the living plant or animal cell. It is a tripeptide with a gamma peptide linkage between the amine group of cysteine (which is attached by normal peptide linkage to a glycine) and the carboxyl group of the glutamate side-chain. It is an antioxidant, preventing damage to important cellular components caused by reactive oxygen species such as free radicals and peroxides. The sulfhydryl (thiol) group (SH) of cysteine serves as a proton donor and is responsible for the biological activity of glutathione.
Glutathione suppresses human immunodeficiency virus expression in chronically infected monocytic cells. It is a useful tripeptide involved in many aspects of metabolism, including transport of g-glutanyl amino acids and reductive cleavage of disulfide bonds.
Endogenous antioxidant that plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Glutathione-S-transferase catalyzes the formation of glutathione thioethers with xenobiotics, leukotrienes, and other molecules that have an electrophilic center. Glutathione also forms disulfide bonds with cysteine residues in proteins. Via these mechanisms, it can have the paradoxical effect of reducing the efficacy of anti-cancer agents.

Fornitore: Apollo Scientific

Descrizione: 2-O-(Carboxymethyl)-D-glucose ≥95%

Fornitore: Apollo Scientific

Descrizione: 3-(Carboxymethyl)-2-fluorobenzeneboronic acid

Fornitore: Apollo Scientific

Descrizione: 4-(Carboxymethyl)-2-fluorobenzeneboronic acid

Fornitore: Apollo Scientific

Descrizione: 3-(Carboxymethyl)benzoic acid 95%

Fornitore: Apollo Scientific

Descrizione: 3-(Carboxymethyl)phenylboronic acid 98%

Codice catalogo: (C6206-25MG)

Fornitore: SIGMA ALDRICH MICROSCOPY

Codice articolo fornitore: C6206-25MG

Codice articolo locale: SIAMC6206-25MG

Descrizione: N-Carboxymethyl-6-(2,2-dicyanovinyl)-1,2,3,4-tetrahydroquinoline. ≥98% (HPLC) (CDCQ)

UOM: 1 * 25 mg

Promo

Fornitore: Apollo Scientific

Descrizione: 2,3,6-Tri-O-(carboxymethyl)-D-glucose ≥95%

Fornitore: TCI

Descrizione: Bis(carboxymethyl)trithiocarbonate ≥98.0% (by titrimetric analysis)

Fornitore: TCI

Descrizione: Tetrasodium-N,N-bis(carboxymethyl)-L-glutamate ∼40% in water