U heeft gezocht op: Glycine+sulphate

Leverancier: Thermo Fisher Scientific

Omschrijving: Strontium sulphate ≥99.9965% (metals basis), Puratronic®

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Leverancier: Thermo Fisher Scientific

Omschrijving: Cesium sulphate ≥99.99% (metals basis)

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Leverancier: Thermo Fisher Scientific

Omschrijving: Lithium sulphate, anhydrous ≥99.7% (metals basis)

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Catalogus nummer: (TCIAP0173-25G)

Leverancier: TCI

Omschrijving: 1,2-Phenylenediamine sulphate ≥97.0% (by titrimetric analysis)

UOM: 1 * 25 g

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Leverancier: Thermo Fisher Scientific

Omschrijving: Cesium sulphate ≥99.9% (metals basis)

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Catalogus nummer: (USBIC9001-21)

Leverancier: US Biological

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

UOM: 1 * 1 EA

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Leverancier: Thermo Fisher Scientific

Omschrijving: N,N-Diethyl-p-phenylenediammonium sulphate 99%

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Leverancier: Thermo Fisher Scientific

Omschrijving: Yttrium(III) sulphate octahydrate ≥97%

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Catalogus nummer: (BOSSBS-13370R-A750)

Leverancier: Bioss

Omschrijving: 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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Catalogus nummer: (BOSSBS-13370R-A680)

Leverancier: Bioss

Omschrijving: 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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Leverancier: Thermo Fisher Scientific

Omschrijving: Adenine sulphate (synthetic) 98%

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Catalogus nummer: (1.09872.0001)

Leverancier: Merck

Omschrijving: Titrisol® standards are traceable to standard reference material from NIST.

UOM: 1 * 1 Ampul

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Leverancier: Apollo Scientific

Omschrijving: Tobramycin is an aminoglycoside antibiotic and hasa bactericidal action against many gram-negative bacteria.

Catalogus nummer: (ENZOALX370009M005)

Leverancier: ENZO LIFE SCIENCES

Omschrijving: PKC activator.

UOM: 1 * 5 mg

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Catalogus nummer: (BOSSBS-13370R-HRP)

Leverancier: Bioss

Omschrijving: 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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Leverancier: Merck

Omschrijving: Calcium sulphate dihydrate, EMSURE® for analysis, precipitated, Supelco®

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