Votre recherche pour: N-Fmoc-glycine

Numéro de catalogue: (BOSSBS-13370R)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13370R-A488)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Numéro de catalogue: (ABCAAB228541-100)

Fournisseur: Abcam

Description: Rabbit polyclonal to alpha 1 Glycine Receptor/GLRA1.

UOM: 1 * 100 µl

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Numéro de catalogue: (USBIG8167-03A)

Fournisseur: US Biological

Description: Anti-Glycine Receptor alpha 3 subunit Rabbit Polyclonal Antibody

UOM: 1 * 1 EA

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Numéro de catalogue: (BOSSBS-13370R-CY3)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13370R-FITC)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Numéro de catalogue: (TCIAC0333-1G)

Fournisseur: TCI

Description: N-Carbobenzoxyglycine 4-nitrophenyl ester ≥98.0% (par HPLC)

UOM: 1 * 1 g

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Fournisseur: TCI

Description: Oxfenicine ≥99.0% (par HPLC, analyse par titration)

Fournisseur: Thermo Fisher Scientific

Description: N-Benzyloxycarbonylglycine ≥98%

MSMD Certificats

Numéro de catalogue: (ABCAAB232989-100)

Fournisseur: Abcam

Description: Rabbit polyclonal to Glycine decarboxylase.

UOM: 1 * 1 EA

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Numéro de catalogue: (BOSSBS-13370R-A555)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13370R-CY7)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Numéro de catalogue: (USBIG8167-03)

Fournisseur: US Biological

Description: Anti-Glycine Receptor Subunit alpha 1 Mouse Monoclonal Antibody [clone: 9G364]

UOM: 1 * 1 EA

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Numéro de catalogue: (BOSSBS-13370R-A647)

Fournisseur: Bioss

Description: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

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Fournisseur: TCI

Description: N-Benzyloxycarbonylglycine ≥98.0% (par HPLC, analyse par titration)

Numéro de catalogue: (ABCAAB192508-100)

Fournisseur: Abcam

Description: Rabbit polyclonal to alpha 1 Glycine Receptor/GLRA1.

UOM: 1 * 1 EA

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