Hai cercato: genome

Codice catalogo: (BOSSBS-15095R)

Fornitore: Bioss

Codice articolo fornitore: BS-15095R

Codice articolo locale: BOSSBS-15095R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf144 gene product has been provisionally designated C20orf144 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15090R)

Fornitore: Bioss

Codice articolo fornitore: BS-15090R

Codice articolo locale: BOSSBS-15090R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15091R)

Fornitore: Bioss

Codice articolo fornitore: BS-15091R

Codice articolo locale: BOSSBS-15091R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf117 gene product has been provisionally designated C20orf117 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15096R)

Fornitore: Bioss

Codice articolo fornitore: BS-15096R

Codice articolo locale: BOSSBS-15096R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15103R)

Fornitore: Bioss

Codice articolo fornitore: BS-15103R

Codice articolo locale: BOSSBS-15103R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf187 gene product has been provisionally designated C20orf187 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-1256R)

Fornitore: Bioss

Codice articolo fornitore: BS-1256R

Codice articolo locale: BOSSBS-1256R

Descrizione: The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its oncogenic transforming activity. This gene and FGF3, another oncogenic growth factor, are located closely on chromosome 11. Co-amplification of both genes was found in various kinds of human tumors. Studies on the mouse homolog suggested a function in bone morphogenesis and limb development through the sonic hedgehog (SHH) signaling pathway. [provided by RefSeq].

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9697R)

Fornitore: Bioss

Codice articolo fornitore: BS-9697R

Codice articolo locale: BOSSBS-9697R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf194 gene product has been provisionally designated C20orf194 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9692R)

Fornitore: Bioss

Codice articolo fornitore: BS-9692R

Codice articolo locale: BOSSBS-9692R

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf111 gene product has been provisionally designated C20orf111 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-11284R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-11284R-CY7

Codice articolo locale: BOSSBS-11284R-CY7

Descrizione: KSP37 is a 223 amino acid protein that is secreted into the extracellular space and belongs to the fibroblast growth factor-binding protein family. Expressed in serum, as well as in cytotoxic T lymphocytes and peripheral leukocytes, KSP37 is thought to be involved in lymphocyte-mediated immunity, possibly playing a role in the development of asthma. The gene encoding KSP37 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15113R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-15113R-FITC

Codice articolo locale: BOSSBS-15113R-FITC

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf7 gene product has been provisionally designated C20orf7 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15115R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15115R-CY3

Codice articolo locale: BOSSBS-15115R-CY3

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf72 gene product has been provisionally designated C20orf72 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15118R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-15118R-HRP

Codice articolo locale: BOSSBS-15118R-HRP

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf79 gene product has been provisionally designated C20orf79 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15118R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15118R-CY7

Codice articolo locale: BOSSBS-15118R-CY7

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf79 gene product has been provisionally designated C20orf79 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15107R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15107R-CY3

Codice articolo locale: BOSSBS-15107R-CY3

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf26 gene product has been provisionally designated C20orf26 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15190R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-15190R-FITC

Codice articolo locale: BOSSBS-15190R-FITC

Descrizione: C4orf29 (chromosome 4 open reading frame 29) is a 414 amino acid secreted protein that exists as four alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15111R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-15111R-FITC

Codice articolo locale: BOSSBS-15111R-FITC

Descrizione: Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf4 gene product has been provisionally designated C20orf4 pending further characterization.

UOM: 1 * 100 µl

Promo