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Catalog Number: (USBIC0115-02Y)
Supplier: US Biological
Description: Anti-Calcitonin Gene-Related Peptide Rabbit Polyclonal Antibody
UOM: 1 * 100 µl


Catalog Number: (USBIP9102-70J)
Supplier: US Biological
Description: Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody
UOM: 1 * 100 µl


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Catalog Number: (USBIC0115-03D)
Supplier: US Biological
Description: Anti-Calcitonin Gene Related Peptide 2 Rabbit polyclonal antibody unconjugated
UOM: 1 * 400 µG


Catalog Number: (USBIN2915-52N)
Supplier: US Biological
Description: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody
UOM: 1 * 200 µl


Catalog Number: (USBIN2915-52N-BIOT)
Supplier: US Biological
Description: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody (Biotin)
UOM: 1 * 200 µl


Catalog Number: (USBII7662-94B-100)
Supplier: US Biological
Description: Anti-Interferon Stimulating Gene 15 Mouse Monoclonal Antibody [clone: 7G32]
UOM: 1 * 100 µl


Catalog Number: (USBIP9102-71H)
Supplier: US Biological
Description: Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 9L604]
UOM: 1 * 200 µl


Catalog Number: (BOSSBS-15518R-A555)
Supplier: Bioss
Description: IFITM5 is a membrane protein thought to play a role in bone mineralisation. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-6338R-HRP)
Supplier: Bioss
Description: This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is thought to play a role in lipid metabolism. Polymorphisms in this gene may influence circulating lipid levels and may be associated with coronary artery disease risk. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring downstream apolipoprotein C-II (APOC2) gene.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-6338R-A680)
Supplier: Bioss
Description: This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is thought to play a role in lipid metabolism. Polymorphisms in this gene may influence circulating lipid levels and may be associated with coronary artery disease risk. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring downstream apolipoprotein C-II (APOC2) gene.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-6338R-A350)
Supplier: Bioss
Description: This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is thought to play a role in lipid metabolism. Polymorphisms in this gene may influence circulating lipid levels and may be associated with coronary artery disease risk. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring downstream apolipoprotein C-II (APOC2) gene.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-0394R)
Supplier: Bioss
Description: This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the regulation of cartilage differentiation. It could also be involved in chondrodysplasias or other cartilage disorders.
UOM: 1 * 100 µl


Supplier: ENZO LIFE SCIENCES
Description: PATHO-GENE® HPV type 16/18/31/33/51 probe is a mixture of biotin-labeled HPV-16, HPV- 18, HPV-31, HPV-33 and HPV-51 specific probes in buffered formamide and hybridisation enhancers.

New Product

Supplier: ENZO LIFE SCIENCES
Description: The PATHO-GENE® HPV type 6/11 probe is a mixture of biotin-labeled HPV 6 and HPV 11-specific probes in buffered formamide and hybridisation enhancers.

New Product

Catalog Number: (BOSSBS-3999R-HRP)
Supplier: Bioss
Description: Summary: This gene encodes a member of the p34Cdc2 protein kinase family. p34Cdc2 kinase family members are known to be essential for eukaryotic cell cycle control. This gene is in close proximity to CDC2L2, a nearly identical gene in the same chromosomal region. The gene loci including this gene, CDC2L2, as well as metalloprotease MMP21/22, consist of two identical, tandemly linked genomic regions which are thought to be a part of the larger region that has been duplicated. This gene and CDC2L2 were shown to be deleted or altered frequently in neuroblastoma with amplified MYCN genes. The protein kinase encoded by this gene could be cleaved by caspases and was demonstrated to play roles in cell apoptosis. Several alternatively spliced variants of this gene have been reported. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-3999R)
Supplier: Bioss
Description: Summary: This gene encodes a member of the p34Cdc2 protein kinase family. p34Cdc2 kinase family members are known to be essential for eukaryotic cell cycle control. This gene is in close proximity to CDC2L2, a nearly identical gene in the same chromosomal region. The gene loci including this gene, CDC2L2, as well as metalloprotease MMP21/22, consist of two identical, tandemly linked genomic regions which are thought to be a part of the larger region that has been duplicated. This gene and CDC2L2 were shown to be deleted or altered frequently in neuroblastoma with amplified MYCN genes. The protein kinase encoded by this gene could be cleaved by caspases and was demonstrated to play roles in cell apoptosis. Several alternatively spliced variants of this gene have been reported. [provided by RefSeq, Jul 2008].
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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