14623 Results for: "3-(Aminomethyl)-2-bromothiophene+hydrochloride"

Supplier: Aviva Systems Biology

Anti-GCSH Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody

Supplier: Abgent

Anti-GCSH Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody (Biotin)

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody (APC (Allophycocyanin))

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody (PE (Phycoerythrin))

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Supplier: US Biological

Anti-GCSH Rabbit Polyclonal Antibody (AP (Alkaline Phosphatase))

Supplier: US Biological

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

Supplier: Abnova

Anti-GCSH Mouse Polyclonal Antibody

Supplier: Honeywell Chemicals

Organic Standard, R1266 Ternidazole HCL, Pack type: Glass Bottle

Supplier: Abnova

Anti-GCSH Mouse Monoclonal Antibody [clone: M2]

Supplier: Abnova

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

Supplier: ProSci Inc.

Anti-GLDC Rabbit Polyclonal Antibody

Supplier: Honeywell Chemicals

Organic Standard, Doxycycline hyclate, Pack type: Glass bottle

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

A natural protease inhibitor for trypsin, papain and cathepsins A and B.

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: EHRENSTORFER

100 µg/mL in Acetonitrile:Dimethyl sulfoxide 1 * 1 mL

Supplier: EHRENSTORFER

100 µg/mL in Acetonitrile:Dimethyl sulfoxide 1 * 1 mL

Supplier: Merck

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