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Product Image-112-0212

Cold resistant gloves, ActivArmr® 78-101

Supplier: Ansell
Description: These ambidextrous, light and stretchable thermal protection gloves are made of special hollow-core Thermolite® fibres which provide a very good thermal insulation barrier between the skin and the surrounding environment.

Image Unavailable-ANTIA98583-100

Anti-Transmembrane Protein 101 Rabbit Polyclonal Antibody

Catalog Number: (ANTIA98583-100)
Supplier: ANTIBODIES.COM
Description: Rabbit polyclonal antibody to TMEM101 for WB and ELISA with samples derived from human and mouse.
UOM: 1 * 100 µG

New Product


Image Unavailable-BOSSBS-9498R-A750

Anti-C9orf153 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-9498R-A750)
Supplier: Bioss
Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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 leukaemias.
UOM: 1 * 100 µl
Product Image-HEATHS14522

Weighing dishes, aluminium

Catalog Number: (HEATHS14522)
Supplier: HEATHROW
Description: Weighing dishes, made from light gauge aluminium are designed for moisture determination balances. Ideal for general-purpose weighing and dispensing.
UOM: 1 * 50 items
Product Image-221-0096

Funnels with short stem, Nalgene®

Catalog Number: (221-0096)
Supplier: Thermo Fisher Scientific
Description: LDPE, transparent.
UOM: 1 * 2 items

Environmentally Preferable


Image Unavailable-BOSSBS-9498R-CY7

Anti-C9ORF153 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-9498R-CY7)
Supplier: Bioss
Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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 characterized 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.
UOM: 1 * 100 µl
Product Image-KING060205/9500086

Sponges, Spontex®

Catalog Number: (KING060205/9500086)
Supplier: KING DISPOSABLES
Description: These sponges are made from 100% natural and cellulose.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-9498R-HRP

Anti-C9ORF153 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-9498R-HRP)
Supplier: Bioss
Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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 characterized 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.
UOM: 1 * 100 µl
Image Unavailable-13152-6X2.5KG

Magnesium chloride hexahydrate 99-101%, Puriss., meets analytical specification of BP, FCC, Ph. Eur., E511 (max. 0.0001% Al), Fluka™

Supplier: Honeywell Chemicals
Description: Magnesium chloride hexahydrate 99-101%, Puriss., meets analytical specification of BP, FCC, Ph. Eur., E511 (max. 0.0001% Al), Fluka™

MSDS

Product Image-HACH42453

Buffer solutions for hardness testing

Supplier: Hach
Description: This buffer is used for hardness and chelant determination by titration.

Image Unavailable-PRSI76-934

Anti-SDC1 Mouse Monoclonal Antibody [clone: DL-101] (PE (Phycoerythrin))

Catalog Number: (PRSI76-934)
Supplier: ProSci Inc.
Description: The DL-101 monoclonal antibody specifically reacts with human CD138, a 85-92 kDa type I heparan sulfate proteoglycan. CD138 is known as Syndecan-1 and is expressed on pre-B cells, immature B cells, plasma cells, and malignant plasma cells, to the exclusion of mature circulating B cells. Syndecan-1 is also expressed on vascular smooth muscle, endothelial, neural, and embryonic mesenchymal cells. It is involved in cellular proliferation, cellular migration, and acts as an extracellular matrix receptor. Among the hematopoietic elements, CD138 is a useful marker for plasma cells.
UOM: 1 * 25 Tests

New Product


Image Unavailable-ROTH4434.1

Ethyl phenylacetate

Catalog Number: (ROTH4434.1)
Supplier: Roth Carl
Description: Ethyl phenylacetate
UOM: 1 * 1 g

Market Source Item This is a MarketSource item. Additional charges may apply

Product Image-80.625

Transport swabs

Catalog Number: (80.625)
Supplier: SARSTEDT
Description: Transport swabs are neutral which is for use on intact skin and in natural body openings.
UOM: 1 * 500 items

Market Source Item This is a MarketSource item. Additional charges may apply

Image Unavailable-BOSSBS-9498R-FITC

Anti-C9ORF153 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-9498R-FITC)
Supplier: Bioss
Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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 characterized 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9498R-A555

Anti-C9ORF153 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-9498R-A555)
Supplier: Bioss
Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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 characterized 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.
UOM: 1 * 100 µl
Product Image-214-1343

Flasks acc. to Kjeldahl

Catalog Number: (214-1343)
Supplier: Kavalier
Description: Borosilicate glass 3.3.
UOM: 1 * 1 items
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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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