Hai cercato: genome

Codice catalogo: (BOSSBS-7013R)

Fornitore: Bioss

Codice articolo fornitore: BS-7013R

Codice articolo locale: BOSSBS-7013R

Descrizione: The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene appears not to be involved in this type of chromosome translocation. Two transcript variants encoding distinct isoforms have been identified for this gene.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-3990R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-3990R-HRP

Codice articolo locale: BOSSBS-3990R-HRP

Descrizione: This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-7013R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-7013R-A350

Codice articolo locale: BOSSBS-7013R-A350

Descrizione: The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene appears not to be involved in this type of chromosome translocation. Two transcript variants encoding distinct isoforms have been identified for this gene.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-12036R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-12036R-CY7

Codice articolo locale: BOSSBS-12036R-CY7

Descrizione: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-12036R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-12036R-FITC

Codice articolo locale: BOSSBS-12036R-FITC

Descrizione: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9368R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-9368R-A350

Codice articolo locale: BOSSBS-9368R-A350

Descrizione: OCEL1, is a 264 amino acid protein that is encoded by a gene which maps to human chromosome 19. Chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin (Ig) superfamily members, including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family and Fc receptors (FcRs). Key genes for eye color and hair color also map to chromosome 19.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-3990R-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-3990R-A647

Codice articolo locale: BOSSBS-3990R-A647

Descrizione: This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-3990R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-3990R-A555

Codice articolo locale: BOSSBS-3990R-A555

Descrizione: This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-12036R-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-12036R-A647

Codice articolo locale: BOSSBS-12036R-A647

Descrizione: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-12036R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-12036R-A350

Codice articolo locale: BOSSBS-12036R-A350

Descrizione: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9473R)

Fornitore: Bioss

Codice articolo fornitore: BS-9473R

Codice articolo locale: BOSSBS-9473R

Descrizione: The product of this gene is a member of the nuclear factors of activated T cells family of transcription factors. Proteins belonging to this family play a central role in inducible gene transcription during the immune response. This protein regulates gene expression induced by osmotic stress in mammalian cells. Unlike monomeric members of this protein family, this protein exists as a homodimer and forms stable dimers with DNA elements. Multiple transcript variants encoding different isoforms have been found for this gene.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13113R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-13113R-CY7

Codice articolo locale: BOSSBS-13113R-CY7

Descrizione: This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transcriptional activators or repressors of numerous genes, and are involved in stem cell development, cell senescence and death, and tumorigenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9473R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-9473R-CY3

Codice articolo locale: BOSSBS-9473R-CY3

Descrizione: The product of this gene is a member of the nuclear factors of activated T cells family of transcription factors. Proteins belonging to this family play a central role in inducible gene transcription during the immune response. This protein regulates gene expression induced by osmotic stress in mammalian cells. Unlike monomeric members of this protein family, this protein exists as a homodimer and forms stable dimers with DNA elements. Multiple transcript variants encoding different isoforms have been found for this gene.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5937R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-5937R-CY3

Codice articolo locale: BOSSBS-5937R-CY3

Descrizione: This gene encodes a mitochondrial outer membrane protein. It has a potential role in tumorigenesis, which may result from negative regulation of the p53 tumor suppressor gene. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Aug 2011].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-11356R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-11356R-A750

Codice articolo locale: BOSSBS-11356R-A750

Descrizione: The protein encoded by this gene is a RAS gene superfamily member that regulates synaptic vesicle exocytosis. This gene also plays a role in the regulation of voltage-gated calcium channels during neurotransmitter and insulin release. Mutations have suggested a role cognition and have been identified as the cause of cone-rod dystrophy type 7. Multiple transcript variants encoding different isoforms have been described for this gene.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-0028R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-0028R-A750

Codice articolo locale: BOSSBS-0028R-A750

Descrizione: The protein encoded by this gene is a serine-threonine kinase, belonging to the glycogen synthase kinase subfamily. It is involved in energy metabolism, neuronal cell development, and body pattern formation. Polymorphisms in this gene have been implicated in modifying risk of Parkinson disease, and studies in mice show that overexpression of this gene may be relevant to the pathogenesis of Alzheimer disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

UOM: 1 * 100 µl

Promo