Sie suchten nach: Glycin+(H-Gly-OH)

Artikel-Nr: (C6331-1MG)

Lieferant: SIGMA ALDRICH MICROSCOPY

Beschreibung: Fluorescent label for amino acids allows for detection of alanine, arginine, glycine, glutamic and aspartic acid in the 0.8-4.5 × 10-18 M range.

UOM: 1 * 1 mg

Aktion

Artikel-Nr: (8.14621.0025)

Lieferant: Merck

Beschreibung: 4-Aminohippursäure, Sigma-Aldrich®

UOM: 1 * 25 g

Sicherheitsdatenblätter Zertifikate Aktion

Lieferant: Apollo Scientific

Beschreibung: Ethyl-N-(diphenylmethylen)glycinat

Lieferant: VWR Chemicals

Beschreibung: Biologischer Puffer für Zellkultur "in vitro", Enzymassays und einige Elektrophoreseanwendungen bei physiologischem pH.

Sicherheitsdatenblätter Zertifikate

Artikel-Nr: (87973.180)

Lieferant: VWR Chemicals

Beschreibung: 4-Aminohippursäure Reag. Ph. Eur. 1003701

UOM: 1 * 100 mL

Sicherheitsdatenblätter Zertifikate Aktion

Artikel-Nr: (32031.297)

Lieferant: VWR Chemicals

Beschreibung: Vorbereitete Lösungen aus AnalaR® NORMAPUR® analytischen Reagenzien.

UOM: 1 * 1 L

Sicherheitsdatenblätter Zertifikate Aktion

Artikel-Nr: (BOSSBS-13370R)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13370R-A488)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (ABCAAB97628-50)

Lieferant: Abcam

Beschreibung: Anti-alpha 2 Glycine Receptor Rabbit Polyclonal Antibody

UOM: 1 * 50 µl

Aktion

Artikel-Nr: (USBIG8167-02)

Lieferant: US Biological

Beschreibung: Anti-Glycine Receptor alpha 1/2 Rabbit polyclonal antibody

UOM: 1 * 200 µG

Aktion

Artikel-Nr: (BOSSBS-13370R-CY3)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13370R-FITC)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (USBIG8167-03)

Lieferant: US Biological

Beschreibung: Anti-Glycine Receptor Subunit alpha 1 Mouse monoclonal antibody [clone: 9G364]

UOM: 1 * 100 µG

Aktion

Artikel-Nr: (USBIG8167-03A)

Lieferant: US Biological

Beschreibung: Anti-Glycine Receptor alpha 3 subunit Rabbit polyclonal antibody

UOM: 1 * 100 µG

Aktion

Lieferant: Thermo Fisher Scientific

Beschreibung: Glycinpropylester Hydrochlorid

Sicherheitsdatenblätter Zertifikate

Lieferant: SIGMA ALDRICH MICROSCOPY

Beschreibung: Benzophenone imine plays a vital role as an ammonia surrogate. It is primarily used as ammonia equivalents for the selective formation of protected primary amines. Benzophenone imine is useful as a synthetic intermediate, especially for the synthesis of glycine Schiff base. Benzophenone imine is useful for the preparation of nitrile yield dimers.