7599 Results for: "(S)-3-(Aminomethyl)-1-boc-piperidine"

Supplier: Abnova

Anti-GCSH Mouse Polyclonal Antibody

Supplier: Thermo Fisher Scientific

Ethyl-2-oxopyrrolidine-3-carboxylate 95%

Supplier: Abnova

Anti-GCSH Mouse Monoclonal Antibody [clone: M2]

Supplier: Thermo Fisher Scientific

(R)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxylic acid 95%

Supplier: Thermo Fisher Scientific

Di-tert-butyl iminodicarboxylate 98%

Supplier: Abnova

Anti-GCSH Mouse Monoclonal Antibody [clone: 3D8-A12]

Supplier: ProSci Inc.

Anti-GLDC Rabbit Polyclonal Antibody

Supplier: Apollo Scientific

Selectively inhibits members of Cystein protease family including Cathepsin L and members of Serine protease family including Subtilisin, Carlsberg and Thermitase

Supplier: Thermo Fisher Scientific

1-tert-Butyl-3-methylpiperazine-1,3-dicarboxylate

Supplier: Thermo Fisher Scientific

Ethyl-4-oxo-3-piperidinecarboxylate hydrochloride 97%

Supplier: Honeywell Chemicals

High quality inorganic and organic reference materials produced according to ISO 9001.

Supplier: Thermo Fisher Scientific

4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy (4-hydroxy-TEMPO, TEMPOL) ≥98% free radical

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Thermo Fisher Scientific

N-(tert-Butoxycarbonyl)-L-valine N'-methoxy-N'-methylamide 97%

Supplier: Antibodies.com

Rat Glycine Decarboxylase ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Glycine Decarboxylase in tissue homogenates, cell lysates or other biological fluids.

Supplier: Antibodies.com

Mouse Glycine Decarboxylase ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Glycine Decarboxylase in tissue homogenates, cell lysates or other biological fluids.

Supplier: Antibodies.com

Human Glycine Decarboxylase ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Glycine Decarboxylase in tissue homogenates, cell lysates or other biological fluids.

Supplier: Merck

(+/-)-5-AMINO-1,3,3-TRIMETHYLCYCLOHEXANE -METHYLAMINE, 99+% 1 * 1 L

Supplier: Merck

1-PYRENEMETHYLAMINE HYDROCHLORIDE, 95% 1 * 1 g

Supplier: Merck

CARBONYL CYANIDE 3-CHLOROPHENYLHYDRAZ& 1 * 1 mg

Supplier: Merck

1-PYRENEMETHYLAMINE HYDROCHLORIDE, 95% 1 * 5 g