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Varenummer: (1.01910.9010)
Leverandør: Merck
Beskrivelse: Bicin, Millipore®
UOM: 1 * 10 kg

MSDS


Varenummer: (C6331-1MG)
Leverandør: SIGMA ALDRICH MICROSCOPY
Beskrivelse: 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


Varenummer: (8.14621.0025)
Leverandør: Merck
Beskrivelse: 4-Aminohippursyre, Sigma-Aldrich®
UOM: 1 * 25 g

Varenummer: (87973.180)
Leverandør: VWR Chemicals
Beskrivelse: 4-Aminohippursyre Reag. Ph. Eur. 1003701
UOM: 1 * 100 mL

Leverandør: VWR Chemicals
Beskrivelse: Biological buffers are useful for cell culture <i>in vitro</i>, enzyme assays and some electrophoretic applications at physiological pH.
Varenummer: (32031.297)
Leverandør: VWR Chemicals
Beskrivelse: Solutions prepared from AnalaR® NORMAPUR® grade analytical reagents.
UOM: 1 * 1 L

Varenummer: (ABCAAB97628-50)
Leverandør: Abcam
Beskrivelse: Anti-alpha 2 Glycine Receptor Rabbit Polyclonal Antibody
UOM: 1 * 50 µl


Varenummer: (USBIG8167-02)
Leverandør: US Biological
Beskrivelse: Anti-Glycine Receptor alpha 1/2 Rabbit polyclonal antibody
UOM: 1 * 1 Each


Varenummer: (BOSSBS-13370R)
Leverandør: Bioss
Beskrivelse: 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


Varenummer: (BOSSBS-13370R-A488)
Leverandør: Bioss
Beskrivelse: 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


Leverandør: Thermo Fisher Scientific
Beskrivelse: Glycinemethylester, HCl 98%
Leverandør: Thermo Fisher Scientific
Beskrivelse: Glycinemethylester, HCl ≥99%
Leverandør: Thermo Fisher Scientific
Beskrivelse: Glycinethylester, HCl ≥99%
Varenummer: (BOSSBS-13370R-FITC)
Leverandør: Bioss
Beskrivelse: 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


Varenummer: (BOSSBS-13370R-CY3)
Leverandør: Bioss
Beskrivelse: 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


Varenummer: (ABCAAB9442-500)
Leverandør: Abcam
Beskrivelse: Anti-Glycine Rabbit Polyclonal Antibody
UOM: 1 * 500 µl


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