You Searched For: VWRA141-1444


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Catalog Number: (SCOI285213622)
Supplier: SI Analytics
Description: Titration head, TZ 1461, for COD sample rack TZ 1444, For: TW alpha plus sample changer
UOM: 1 * 1 items


Supplier: Thermo Fisher Scientific
Description: 2-Phenylcyclohexanone 98

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Supplier: Apollo Scientific
Description: 1,2-Cyclohexanedicarboximide 95%

Catalog Number: (APOSOR110447-1G)
Supplier: Apollo Scientific
Description: Methyl 1-methyl-1H-indole-4-carboxylate
UOM: 1 * 1 g


Catalog Number: (HITA810-1444)
Supplier: VWR Collection
Description: Pushing screw 1 * 1 items
UOM: 1 * 1 items


Supplier: Thermo Fisher Scientific
Description: Acetamidine hydrochloride 97
Catalog Number: (H64317.06)
Supplier: Thermo Fisher Scientific
Description: 1-Bromo-4-fluorobutane 97%
UOM: 1 * 5 g

Catalog Number: (B22330.14)
Supplier: Thermo Fisher Scientific
Description: 3-Methyl-2-butanethiol 95% remainder mainly 2-methyl-1-butanethiol
UOM: 1 * 25 g

MSDS


Supplier: Thermo Fisher Scientific
Description: (2-Bromoethoxy)-tert-butyldimethylsilane 98% Stabilised

Supplier: Thermo Fisher Scientific
Description: (±)-γ-Octalactone 98
Supplier: Thermo Fisher Scientific
Description: Ammonium peroxodisulphate (APS) 98
Supplier: Thermo Fisher Scientific
Description: Ammonium peroxodisulphate (APS) ≥98.0% ACS
Supplier: Thermo Scientific
Description: Designed for everyday laboratory needs the Thermo Scientific™ TSG series general purpose laboratory freezers are designed with your needs in mind. The TSG series range of freezers feature the performance, security, and quality required for your laboratory applications.

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Catalog Number: (BOSSBS-15344R-HRP)
Supplier: Bioss
Description: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf84 gene product has been provisionally designated C9orf84 pending further characterisation. There are two isoforms of C9orf84 that are produced as a result of alternative splicing events.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-15344R-CY5)
Supplier: Bioss
Description: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf84 gene product has been provisionally designated C9orf84 pending further characterisation. There are two isoforms of C9orf84 that are produced as a result of alternative splicing events.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-15344R-A680)
Supplier: Bioss
Description: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf84 gene product has been provisionally designated C9orf84 pending further characterisation. There are two isoforms of C9orf84 that are produced as a result of alternative splicing events.
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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