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Wyszukano: (2-Fluorophenyl)glycine


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Producent: Thermo Fisher Scientific
Opis: Chlorowodorek estru etylowego glicyny ≥99%
Producent: Thermo Fisher Scientific
Opis: Ester tert-butylowy glicyny ≥97%
Numer katalogowy: (USBIC9001-21)
Producent: US Biological
Opis: Anti-Cysteine and Glycine-rich Protein 3 Chicken Polyclonal Antibody
j.m.: 1 * 50 µG


Numer katalogowy: (USBIG8167-03)
Producent: US Biological
Opis: Anti-Glycine Receptor Subunit alpha 1 Mouse monoclonal antibody [clone: 9G364]
j.m.: 1 * 100 µG


Numer katalogowy: (BOSSBS-13370R)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13370R-A488)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Producent: Thermo Fisher Scientific
Opis: Chlorowodorek estru metylowego glicyny ≥99%
Producent: Apollo Scientific
Opis: Ester tert-butylowy glicyny 97%

Numer katalogowy: (BOSSBS-13370R-CY7)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13370R-A555)
Producent: Bioss
Opis: 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.
j.m.: 1 * 100 µl


Producent: Apollo Scientific
Opis: Component of tris-glycine-sds running buffers forpolyacrylamide gel electrophoresis.

Numer katalogowy: (APOSOR17705-100G)
Producent: Apollo Scientific
Opis: tert-Butyl-2-((diphenylmethylene)amino)acetate 98%
j.m.: 1 * 100 g


Numer katalogowy: (ACRO297020025)
Producent: Thermo Fisher Scientific
Opis: Chlorowodorek estru tert-butylowego glicyny 99%
j.m.: 1 * 2,5 g

MSDS


Producent: Thermo Fisher Scientific
Opis: Chlorowodorek estru tert-butylowego glicyny ≥99%
Producent: Apollo Scientific
Opis: Phospholipid membrane component, precursor of inositol phosphates

Producent: PanReac AppliChem
Opis: Glicyna
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Zapasy tego artykułu są ograniczone, ale możliwe, że jest on dostępny w pobliskim magazynie. Upewnij się, że jesteś zalogowany na stronie, aby móc sprawdzić dostępność zapasów. Jeśli call ciągle się wyświetla i potrzebujesz pomocy, zadzwoń na 58 323 82 00.
Ten produkt jest ograniczony w dostępie i można go zamówić tylko przy użyciu zaaprobowanego konta. Jeśli potrzebujesz pomocy, napisz do Działu Prawnego VWR na tomasz.chrobak@pl.vwr.com
Do zakupu tego produktu może być potrzebna dodatkowa dokumentacja. Przedstawiciel VWR skontaktuje się z Tobą w razie potrzeby.
Ten produkt jest zablokowany na stronie internetowej. W celu zamówienia, skontaktuj się z Działem Obsługi Klienta.
Produkt oryginalny został wycofany. Dostępny jest wskazny zamiennik .
Wybrany produkt został wycofany - sprzedaż do wyczerpania zapasów. Dostępne zamienniki można znaleźć poprzez wpisanie powyższego numeru katalogowego VWR w okno wyszukiwarki. Jeśli potrzebujesz dalszej pomocy, prosimy o kontakt z Działem Doradztwa Produktowego pod numerem telefonu 58 3238 220.
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