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Description: Anti-Calcitonin Gene-Related Peptide Rabbit Polyclonal Antibody

Catalog Number: USBIC0115-02Y

UOM: 1 * 100 µl

Supplier: US Biological

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Description: Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody

Catalog Number: USBIP9102-70J

UOM: 1 * 100 µl

Supplier: US Biological

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Description: Anti-Calcitonin Gene Related Peptide 2 Rabbit polyclonal antibody unconjugated

Catalog Number: USBIC0115-03D

UOM: 1 * 400 µG

Supplier: US Biological

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Description: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody

Catalog Number: USBIN2915-52N

UOM: 1 * 200 µl

Supplier: US Biological

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Description: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody (Biotin)

Catalog Number: USBIN2915-52N-BIOT

UOM: 1 * 200 µl

Supplier: US Biological

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Description: Anti-Interferon Stimulating Gene 15 Mouse Monoclonal Antibody [clone: 7G32]

Catalog Number: USBII7662-94B-100

UOM: 1 * 100 µl

Supplier: US Biological

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Description: Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 9L604]

Catalog Number: USBIP9102-71H

UOM: 1 * 200 µl

Supplier: US Biological

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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).

Catalog Number: BOSSBS-15518R-A555

UOM: 1 * 100 µl

Supplier: Bioss

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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.

Catalog Number: BOSSBS-6338R-HRP

UOM: 1 * 100 µl

Supplier: Bioss

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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.

Catalog Number: BOSSBS-6338R-A680

UOM: 1 * 100 µl

Supplier: Bioss

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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.

Catalog Number: BOSSBS-6338R-A350

UOM: 1 * 100 µl

Supplier: Bioss

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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.

Catalog Number: BOSSBS-0394R

UOM: 1 * 100 µl

Supplier: Bioss

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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.

Catalog Number: ENZOENZ328826000

UOM: 1 * 6 mL

Supplier: ENZO LIFE SCIENCES

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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.

Catalog Number: ENZOENZ32885

UOM: 1 * 1 mL

Supplier: ENZO LIFE SCIENCES

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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].

Catalog Number: BOSSBS-3999R-HRP

UOM: 1 * 100 µl

Supplier: Bioss

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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].

Catalog Number: BOSSBS-3999R

UOM: 1 * 100 µl

Supplier: Bioss

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