You Searched For: N-Acetyl-DL-alanine


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Catalog Number: (L17671.MD)
Supplier: Alfa Aesar
Description: DL-2-Amino-4-phosphonobutyric acid 95%
UOM: 1 * 250 mg


Catalog Number: (H62256.03)
Supplier: Alfa Aesar
Description: 4-Acetyl-2-fluorobenzeneboronic acid pinacol ester 96%
UOM: 1 * 1 g


Supplier: Alfa Aesar
Description: 5-Acetyl-2,4-dimethylthiazole ≥99%

Catalog Number: (APOSOR919291-5G)
Supplier: APOLLO SCIENTIFIC
Description: 3-Acetyl-1-methyl-1H-pyrrole 95%
UOM: 1 * 5 g


Catalog Number: (APOSOR32252-1G)
Supplier: APOLLO SCIENTIFIC
Description: Methyl-4-acetyl-1H-pyrrole-2-carboxylate 95%
UOM: 1 * 1 g


Supplier: APOLLO SCIENTIFIC
Description: Ac-DL-Pra-Oet 95%

Catalog Number: (APOSOR110286-1G)
Supplier: APOLLO SCIENTIFIC
Description: 2-Acetyl-6-iodo-2H-indazole
UOM: 1 * 1 g


Supplier: APOLLO SCIENTIFIC
Description: 2-Azidoethyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 99% min

Catalog Number: (BOSSBS-11822R-FITC)
Supplier: Bioss
Description: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-11822R-HRP)
Supplier: Bioss
Description: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl


Supplier: APOLLO SCIENTIFIC
Description: 3-Acetyl-5-bromo-2-fluoropyridine 98%

Supplier: Thermo Scientific
Description: DL-Glutamic acid monohydrate 98+%

Supplier: APOLLO SCIENTIFIC
Description: 2-(Trifluoromethyl)-DL-phenylglycine 97%

Supplier: APOLLO SCIENTIFIC
Description: 2-Acetyl-3-(Boc-amino)pyrazine

Catalog Number: (APOSPC302576-1G)
Supplier: APOLLO SCIENTIFIC
Description: 4-Chloro-3,5-difluoro-DL-phenylalanine
UOM: 1 * 1 g


Catalog Number: (H31888.03)
Supplier: Alfa Aesar
Description: Methyl-1,2,3,4-tetra-O-acetyl-β-D-glucuronate 98%
UOM: 1 * 1 g

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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.
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
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The original product is no longer available. The replacement shown is available.
This product is no longer available. 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 88 22222.
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