You Searched For: 3-Bromo-2,6-difluoropyridine


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Supplier: Merck
Description: Tricine, Millipore®
Catalog Number: (1.01910.9010)
Supplier: Merck
Description: Bicine, Millipore®
UOM: 1 * 10 kg

MSDS


Catalog Number: (8.14160.0025)
Supplier: Merck
Description: 2,5-Piperazinedione for synthesis, Sigma-Aldrich®
UOM: 1 * 25 g

MSDS


Catalog Number: (1.09432.1000)
Supplier: Merck
Description: Materials for the precise calibration and monitoring of pH meters.
UOM: 1 * 1 L

Catalog Number: (8.14621.0025)
Supplier: Merck
Description: 4-Aminohippuric acid, Sigma-Aldrich®
UOM: 1 * 25 g

Supplier: VWR Chemicals
Description: Biological buffers are useful for cell culture <i>in vitro</i>, enzyme assays and some electrophoretic applications at physiological pH.
Catalog Number: (USBIG8167-02)
Supplier: US Biological
Description: Anti-Glycine Receptor alpha 1/2 Rabbit Polyclonal Antibody
UOM: 1 * 200 µG


Catalog Number: (BOSSBS-13370R-CY3)
Supplier: Bioss
Description: 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


Catalog Number: (BOSSBS-13370R-FITC)
Supplier: Bioss
Description: 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


Catalog Number: (87973.180)
Supplier: VWR Chemicals
Description: 4-Aminohippuric acid Reag. Ph. Eur. 1003701
UOM: 1 * 100 mL

Catalog Number: (C6331-1MG)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: 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


Catalog Number: (ABCAAB166935-200)
Supplier: Abcam
Description: Anti-alpha 1 Glycine Receptor/GLRA1 Goat Polyclonal Antibody
UOM: 1 * 200 µl


Catalog Number: (ABCAAB97628-50)
Supplier: Abcam
Description: Anti-alpha 2 Glycine Receptor Rabbit Polyclonal Antibody
UOM: 1 * 50 µl


Catalog Number: (ABCAAB228541-100)
Supplier: Abcam
Description: Anti-alpha 1 Glycine Receptor/GLRA1 Rabbit Polyclonal Antibody
UOM: 1 * 100 µl


Catalog Number: (USBIG8167-03A)
Supplier: US Biological
Description: Anti-Glycine Receptor alpha 3 subunit Rabbit Polyclonal Antibody
UOM: 1 * 100 µG


Catalog Number: (BOSSBS-13370R)
Supplier: Bioss
Description: 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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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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