N-Isovaleryl-glycin
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
Glycinethylester Hydrochlorid (H-Gly-OEt.HCl) 98%
Lieferant:
Thermo Scientific
Beschreibung:
Glycinmethylester Hydrochlorid (H-Gly-OMe.HCl) 98%
Lieferant:
Alfa Aesar
Beschreibung:
Glycinethylester Hydrochlorid (H-Gly-OEt.HCl) ≥99%
Artikel-Nr:
(USBIG8167-03A)
Lieferant:
US Biological
Hersteller-Artikelnummer::
G8167-03A
Lokale Artikelnummer::
USBIG8167-03A
Beschreibung:
Anti-Glycine Receptor alpha 3 subunit Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Lieferant:
Alfa Aesar
Beschreibung:
Glycinmethylester Hydrochlorid (H-Gly-OMe.HCl) ≥99%
Lieferant:
Alfa Aesar
Beschreibung:
Glycinpropylester Hydrochlorid
Artikel-Nr:
(C6331-1MG)
Lieferant:
SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer::
C6331-1MG
Lokale Artikelnummer::
SIAMC6331-1MG
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.
VE:
1 * 1 mg
Artikel-Nr:
(BOSSBS-13370R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13370R
Lokale Artikelnummer::
BOSSBS-13370R
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
Lieferant:
Thermo Scientific
Beschreibung:
Glycinethylester Hydrochlorid (H-Gly-OEt.HCl) 99%
Artikel-Nr:
(APOSOR43634-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR43634-100G
Lokale Artikelnummer::
APOSOR43634-100G
Beschreibung:
Glycinethylester Hydrochlorid (H-Gly-OEt.HCl) 98%
VE:
1 * 100 g
Artikel-Nr:
(USBIG8167-03)
Lieferant:
US Biological
Hersteller-Artikelnummer::
G8167-03
Lokale Artikelnummer::
USBIG8167-03
Beschreibung:
Anti-Glycine Receptor Subunit alpha 1 Mouse Monoclonal Antibody [clone: 9G364]
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-13370R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13370R-CY3
Lokale Artikelnummer::
BOSSBS-13370R-CY3
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
Artikel-Nr:
(BOSSBS-13370R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13370R-FITC
Lokale Artikelnummer::
BOSSBS-13370R-FITC
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
Artikel-Nr:
(BOSSBS-13370R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13370R-A488
Lokale Artikelnummer::
BOSSBS-13370R-A488
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Glycinbenzylester Hydrochlorid (H-Gly-OBzl.HCl) 95%
Lieferant:
Thermo Scientific
Beschreibung:
Glycinbenzylester Hydrochlorid (H-Gly-OBzl.HCl) 97%
Preis auf Anfrage
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