Procurou por: N-Fmoc-N-benzyl-glycine

Fornecedor: TCI

Descrição: Tiopronin ≥97.0% (by GC, titration analysis)

Fornecedor: TCI

Descrição: Glicina ≥99.0% (by titrimetric analysis) para eletroforese

Código de Artigo: (BOSSBS-13323R-CY7)

Fornecedor: Bioss

Descrição: 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

Promoção

Código de Artigo: (BOSSBS-1384R-A555)

Fornecedor: Bioss

Descrição: 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

Promoção

Código de Artigo: (BOSSBS-13449R)

Fornecedor: Bioss

Descrição: GLYATL2 is a 294 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL2 can also conjugate a multitude of substrates, including oleoyl-CoA and arachidonoyl-CoA, to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL2 is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

UOM: 1 * 100 µl

Promoção

Fornecedor: Apollo Scientific

Descrição: Biological buffer - useful range 7.6 - 9.0. Recommended for low temperature work.

Fornecedor: TCI

Descrição: 2-((4-Cyanophenyl)amino)acetic acid ≥98.0% (by HPLC, titration analysis)

Código de Artigo: (BOSSBS-13444R-HRP)

Fornecedor: Bioss

Descrição: GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

UOM: 1 * 100 µl

Promoção

Fornecedor: TCI

Descrição: 3,4-Dimethylhippuric acid ≥98.0% (by HPLC, titration analysis)

Fornecedor: Apollo Scientific

Descrição: 3-Methyl-2-thiohydantoin 96%

Fornecedor: Apollo Scientific

Descrição: Ethyl-2-{[3-chloro-5-(trifluoromethyl)-2-pyridinyl]amino}acetate 95%

Código de Artigo: (APOSPC910928-1G)

Fornecedor: Apollo Scientific

Descrição: Ethyl 2-[(3-fluorophenyl)amino]acetate 98%

UOM: 1 * 1 g

Promoção

Fornecedor: TCI

Descrição: Bicina ≥99.0% (by titrimetric analysis) good's buffer component for biological research

Código de Artigo: (BOSSBS-2396R-CY3)

Fornecedor: Bioss

Descrição: 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

Promoção

Código de Artigo: (BOSSBS-1384R)

Fornecedor: Bioss

Descrição: 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

Promoção

Fornecedor: Apollo Scientific

Descrição: Bile salt.

Certificados