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N-Fmoc-N-benzyl-glycine
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N-Fmoc-N-benzyl-glycine
Lieferant:
Thermo Scientific
Beschreibung:
Glycinmethylester Hydrochlorid (H-Gly-OMe.HCl) 98%
Lieferant:
Alfa Aesar
Beschreibung:
Glycinethylester Hydrochlorid (H-Gly-OEt.HCl) ≥99%
Lieferant:
Alfa Aesar
Beschreibung:
Glycinpropylester Hydrochlorid
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
Lieferant:
Alfa Aesar
Beschreibung:
Glycinmethylester Hydrochlorid (H-Gly-OMe.HCl) ≥99%
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)
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
Artikel-Nr:
(BOSSBS-13370R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13370R-CY7
Lokale Artikelnummer::
BOSSBS-13370R-CY7
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-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13370R-A555
Lokale Artikelnummer::
BOSSBS-13370R-A555
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
Artikel-Nr:
(32031.297)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC32031.297
Beschreibung:
Vorbereitete Lösungen aus AnalaR® NORMAPUR® Reagenzien zur Analyse.
VE:
1 * 1 L
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:
(ABCAAB228541-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB228541-100
Lokale Artikelnummer::
ABCAAB228541-100
Beschreibung:
Anti-alpha 1 Glycine Receptor/GLRA1 Rabbit Polyclonal Antibody
VE:
1 * 100 µl
 This is a MarketSource item. Additional charges may apply
Lieferant:
Alfa Aesar
Beschreibung:
Tricin ≥98%
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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