47158 Results for: "gene"

Supplier: US Biological

Anti-Interferon Stimulating Gene 15 Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-Calcitonin Gene-Related Peptide Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-Trk-Fused Gene Protein Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-Capillary Morphogenesis Gene 2 Goat Polyclonal Antibody

Supplier: Bioss

A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. This gene is found near this cluster; it was mapped near the gene for C2 within a 120-kb region that included a HSP70 gene pair. These genes are all within the human major histocompatibility complex class III region. This gene was thought to be two different genes, NG36 and G9a, adjacent to each other but a recent publication shows that there is only a single gene. The protein encoded by this gene is thought to be involved in intracellular protein-protein interaction. There are three alternatively spliced transcript variants of this gene but only two are fully described. [provided by RefSeq, Jul 2008].

Supplier: US Biological

Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody

Supplier: ENZO LIFE SCIENCES

Klenow (3′-5′ exo-) is a mesophilic DNA polymerase deficient in both proofreading (3′-5′) and nick-translation (5′-3′) nuclease activities, and that displays a moderate strand displacement activity during DNA synthesis. The protein is expressed as a truncated product of the E.coli PolA gene and contains the D355A and E357A mutations.

Supplier: US Biological

Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody

Supplier: Bioss

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).

Supplier: Bioss

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.

Supplier: US Biological

Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Monoclonal Antibody [clone: 11C1051]

Supplier: US Biological

Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody (FITC (Fluorescein))

Supplier: Bioss

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.

Supplier: Bioss

This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 3. This gene is widely expressed in many tissues, but the exact function of the encoded protein is unknown.

Supplier: Bioss

MAP7D1 (MAP7 Domain Containing 1) is a Protein-Coding gene. Gene Ontology (GO) annotations related to this gene include structural molecule activity. An important paralog of this gene is MAP7.

Supplier: Bioss

This gene encodes an epididymal protease inhibitor, which contains both kunitz-type and WAP-type four-disulfide core (WFDC) protease inhibitor consensus sequences. Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene is a member of the WFDC gene family and belongs to the telomeric cluster. The protein can inhibit human sperm motility, and polymorphisms in this gene are associated with male infertility. Read-through transcription also exists between this gene and the downstream WFDC6 (WAP four-disulfide core domain 6) gene. [provided by RefSeq].

Supplier: US Biological

Anti-Prostate Specific Gene-1 Rabbit Polyclonal Antibody

Supplier: Bioss

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.

Supplier: Bioss

This gene encodes a protein that contains domains of thioredoxin and ERV1, members of two long-standing gene families. The gene expression is induced as fibroblasts begin to exit the proliferative cycle and enter quiescence, suggesting that this gene plays an important role in growth regulation. Two transcript variants encoding two different isoforms have been found for this gene.

Supplier: US Biological

Anti-MHC Class 1 Chain-related Gene A Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Supplier: US Biological

Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 31A3]

Supplier: US Biological

Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 8k263]

Supplier: US Biological

Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 5G201]

Supplier: US Biological

Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 9L605]

Supplier: US Biological

Anti-Calcitonin Gene Related Peptide Mouse Monoclonal Antibody [clone: 2Q2268]

Supplier: US Biological

Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 13C4]

Supplier: Bioss

This gene encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF/p53 pathway. A number of genes are fusion partners have been characterized, in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in this gene are associated with acute myeloid leukemia. More than a dozen pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Nov 2009].

Supplier: Bioss

This gene encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF/p53 pathway. A number of genes are fusion partners have been characterized, in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in this gene are associated with acute myeloid leukemia. More than a dozen pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Nov 2009].

Supplier: Bioss

Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed.