Sie suchten nach: (2-Fluorophenyl)glycine

Lieferant: Thermo Fisher Scientific

Beschreibung: Glycinethylester Hydrochlorid (H-Gly-OEt.HCl) ≥99%

Sicherheitsdatenblätter Zertifikate

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.

VE: 1 * 100 µl

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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.

VE: 1 * 100 µl

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Artikel-Nr: (USBIG8167-03A)

Lieferant: US Biological

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

VE: 1 * 100 µG

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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.

VE: 1 * 100 µl

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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.

VE: 1 * 100 µl

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Artikel-Nr: (ABCAAB9442-500)

Lieferant: Abcam

Beschreibung: Anti-Glycine Rabbit Polyclonal Antibody

VE: 1 * 500 µl

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Lieferant: Thermo Fisher Scientific

Beschreibung: Glycinmethylester Hydrochlorid (H-Gly-OMe.HCl) ≥99%

Sicherheitsdatenblätter Zertifikate

Lieferant: Apollo Scientific

Beschreibung: Glycinbenzylester Hydrochlorid (H-Gly-OBzl.HCl) 95%

Lieferant: Thermo Fisher Scientific

Beschreibung: Glycinpropylester Hydrochlorid

Sicherheitsdatenblätter Zertifikate

Artikel-Nr: (USBIG8167-03)

Lieferant: US Biological

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

VE: 1 * 100 µG

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Lieferant: Thermo Fisher Scientific

Beschreibung: Glycinbenzylester Hydrochlorid (H-Gly-OBzl.HCl) 97%

Sicherheitsdatenblätter

Artikel-Nr: (USBIC9001-21)

Lieferant: US Biological

Beschreibung: Anti-Cysteine and Glycine-rich Protein 3 Chicken Polyclonal Antibody

VE: 1 * 50 µG

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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.

Lieferant: Thermo Fisher Scientific

Beschreibung: Tricin ≥98%

Sicherheitsdatenblätter Zertifikate

Artikel-Nr: (BOSSBS-13370R-A555)

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.

VE: 1 * 100 µl

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