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Varenummer: (BOSSBS-2976R-A555)
Leverandør: Bioss
Beskrivelse: Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates, and other gamma-glutamyl compounds. The metabolism of glutathione releases free glutamate and the dipeptide, cysteinyl-glycine, which is hydrolyzed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyze a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracellular GSH level. It is part of the cell antioxidant defense mechanism. Isoform 3 seems to be inactive.
UOM: 1 * 100 µl


Leverandør: Apollo Scientific
Beskrivelse: Bile salt.
Leverandør: Thermo Fisher Scientific
Beskrivelse: Appearance: White Powder
Leverandør: Apollo Scientific
Beskrivelse: Perfluorbutanesulphonylamide(N-methyl)acetate 97%

Varenummer: (BOSSBS-13323R-A488)
Leverandør: Bioss
Beskrivelse: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-13323R-A647)
Leverandør: Bioss
Beskrivelse: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-1384R-A647)
Leverandør: Bioss
Beskrivelse: Cysteine protease required for the cytoplasm to vacuole transport (Cvt) and autophagy. Cleaves the C-terminal amino acid of ATG8 family proteins MAP1LC3, GABARAPL1, GABARAPL2 and GABARAP, to reveal a C-terminal glycine. Exposure of the glycine at the C-terminus is essential for ATG8 proteins conjugation to phosphatidylethanolamine (PE) and insertion to membranes, which is necessary for autophagy. Has also an activity of delipidating enzyme for the PE-conjugated forms.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-1384R-A750)
Leverandør: Bioss
Beskrivelse: Cysteine protease required for the cytoplasm to vacuole transport (Cvt) and autophagy. Cleaves the C-terminal amino acid of ATG8 family proteins MAP1LC3, GABARAPL1, GABARAPL2 and GABARAP, to reveal a C-terminal glycine. Exposure of the glycine at the C-terminus is essential for ATG8 proteins conjugation to phosphatidylethanolamine (PE) and insertion to membranes, which is necessary for autophagy. Has also an activity of delipidating enzyme for the PE-conjugated forms.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-1384R-A350)
Leverandør: Bioss
Beskrivelse: Cysteine protease required for the cytoplasm to vacuole transport (Cvt) and autophagy. Cleaves the C-terminal amino acid of ATG8 family proteins MAP1LC3, GABARAPL1, GABARAPL2 and GABARAP, to reveal a C-terminal glycine. Exposure of the glycine at the C-terminus is essential for ATG8 proteins conjugation to phosphatidylethanolamine (PE) and insertion to membranes, which is necessary for autophagy. Has also an activity of delipidating enzyme for the PE-conjugated forms.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-1384R-A680)
Leverandør: Bioss
Beskrivelse: Cysteine protease required for the cytoplasm to vacuole transport (Cvt) and autophagy. Cleaves the C-terminal amino acid of ATG8 family proteins MAP1LC3, GABARAPL1, GABARAPL2 and GABARAP, to reveal a C-terminal glycine. Exposure of the glycine at the C-terminus is essential for ATG8 proteins conjugation to phosphatidylethanolamine (PE) and insertion to membranes, which is necessary for autophagy. Has also an activity of delipidating enzyme for the PE-conjugated forms.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-2396R-A555)
Leverandør: Bioss
Beskrivelse: 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.
UOM: 1 * 100 µl


Varenummer: (BOSSBS-2396R-A350)
Leverandør: Bioss
Beskrivelse: 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.
UOM: 1 * 100 µl


Leverandør: TCI
Beskrivelse: 4-Fluorohippuric acid ≥98.0% (by GC, titration analysis)

Leverandør: Thermo Fisher Scientific
Beskrivelse: CAS No.: 16338-48-0
Leverandør: TCI
Beskrivelse: (±)-2-Amino-2-(4-chlorophenyl)acetic acid ≥98.0% (by titrimetric analysis)

Varenummer: (BOSSBS-6233R-CY3)
Leverandør: Bioss
Beskrivelse: NMT2 catalyzes the reaction of N-terminal myristoylation of many signaling proteins. It transfers myristic acid from myristoyl coenzyme A to the amino group of a protein's N-terminal glycine residue. several distinct NMTs exist, varying in apparent molecular weight and /or subcellular distribution.
UOM: 1 * 100 µl


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