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

Fornecedor: Thermo Fisher Scientific

Descrição: Glicina ≥99.5% para eletroforese

MSDS Certificados

Fornecedor: TCI

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

Fornecedor: Thermo Fisher Scientific

Descrição: Ácido 4-Amino-Hipúrico 99%

MSDS

Fornecedor: TCI

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

Fornecedor: Thermo Fisher Scientific

Descrição: Bicina ≥99%

MSDS Certificados

Fornecedor: Thermo Fisher Scientific

Descrição: Glicina 99+% para análise

MSDS

Fornecedor: TCI

Descrição: Noopept ≥98.0% (by HPLC, titration analysis)

Fornecedor: Apollo Scientific

Descrição: Amino(3-hydroxyphenyl)acetic acid hydrochloride 97%

Fornecedor: Apollo Scientific

Descrição: Boc-D-propargylglycine 97%

Código de Artigo: (J62407.A1)

Fornecedor: Thermo Fisher Scientific

Descrição: Glicina ≥99.5% reagente para cultura de célula

UOM: 1 * 1 kg

MSDS Certificados Promoção

Fornecedor: Thermo Fisher Scientific

Descrição: Glicina 98%, extra puro

MSDS

Fornecedor: ENZO LIFE SCIENCES

Descrição: Potent and selective NMDA receptor glycine site antagonist.

Novo produto

Código de Artigo: (BOSSBS-1384R-CY3)

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: TCI

Descrição: Glicina ≥99.0% (by titrimetric analysis)

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-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