You Searched For: Amino(phenyl)acetyl+chloride


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Catalog Number: (F7258-25G)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: Fast green FCF, Sigma-Aldrich®
UOM: 1 * 25 g


Supplier: Thermo Fisher Scientific
Description: CAS No.: 13558-31-1
Supplier: Apollo Scientific
Description: (S)-β-Phenylalaninol 95%

Catalog Number: (APOSOR2650T-250MG)
Supplier: Apollo Scientific
Description: Chemiluminescent with antifilarial & affinity for the adenosine receptor.
UOM: 1 * 250 mg


Catalog Number: (L19802.03)
Supplier: Thermo Fisher Scientific
Description: 3-(Boc-amino)-3-phenylpropionic acid 97%
UOM: 1 * 1 g

Supplier: Apollo Scientific
Description: 3-Amino-4'-(trifluoromethyl)biphenyl hydrochloride

Supplier: Thermo Fisher Scientific
Description: L-Phenylalaninol 98%
Catalog Number: (M6900-50G)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: Methyl Blue is a triaminotriphenylmethane dye, widely used in paper, textile and leather production.
UOM: 1 * 50 g


Catalog Number: (APOSOR307578-1G)
Supplier: Apollo Scientific
Description: 3-tert-Butoxycarbonylamino-3-(3-nitro-phenyl)-propionic acid
UOM: 1 * 1 g


Supplier: Cayman Chemical
Description: Ethyl-2-amino-4-phenylthiophene-3-carboxylate

Supplier: Apollo Scientific
Description: 1-(3-Amino-4-morpholinophenyl)-1-ethanone 95%

Supplier: Apollo Scientific
Description: 2-Amino-2-(4-fluorophenyl)propanoic acid 95%

Catalog Number: (BOSSBS-9219R-HRP)
Supplier: Bioss
Description: MEAF6, also known as Eaf6 or NY-SAR-91, is a 191 amino acid nuclear protein belonging to the EAF6 family. MEAF6 is a component of the NuA4 histone acetyltransferase complex, which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histone H4 and H2A. The gene encoding MEAF6 localizes to chromosome 1 and, due to alternative splicing events, MEAF6 exists in at least three isoforms. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1 such as Hutchinson-Gilford progeria, Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-9219R-A750)
Supplier: Bioss
Description: MEAF6, also known as Eaf6 or NY-SAR-91, is a 191 amino acid nuclear protein belonging to the EAF6 family. MEAF6 is a component of the NuA4 histone acetyltransferase complex, which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histone H4 and H2A. The gene encoding MEAF6 localises to chromosome 1 and, due to alternative splicing events, MEAF6 exists in at least three isoforms. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1 such as Hutchinson-Gilford progeria, Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.
UOM: 1 * 100 µl


Supplier: Apollo Scientific
Description: 3-Amino-1-(4-chlorophenyl)-1H-pyrazole 95%

Catalog Number: (BOSSBS-9219R-A350)
Supplier: Bioss
Description: MEAF6, also known as Eaf6 or NY-SAR-91, is a 191 amino acid nuclear protein belonging to the EAF6 family. MEAF6 is a component of the NuA4 histone acetyltransferase complex, which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histone H4 and H2A. The gene encoding MEAF6 localizes to chromosome 1 and, due to alternative splicing events, MEAF6 exists in at least three isoforms. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1 such as Hutchinson-Gilford progeria, Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.
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.
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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