Hai cercato: genomes

Codice catalogo: (BOSSBS-15105R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-15105R-A750

Codice articolo locale: BOSSBS-15105R-A750

Descrizione: C20orf202 is a 122 amino acid protein that is pending further characterization. The gene encoding C20orf202 maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought to be important for seminal production and may be potential targets for male contraception.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9995R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-9995R-A680

Codice articolo locale: BOSSBS-9995R-A680

Descrizione: C4orf32 is a 132 amino acid single pass membrane protein that 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-4291R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-4291R-CY5

Codice articolo locale: BOSSBS-4291R-CY5

Descrizione: Probable E3 ubiquitin-protein ligase. The BRCA1-BARD1 heterodimer specifically mediates the formation of 'Lys-6'-linked polyubiquitin chains and coordinates a diverse range of cellular pathways such as DNA damage repair, ubiquitination and transcriptional regulation to maintain genomic stability. Plays a central role in the control of the cell cycle in response to DNA damage. Acts by mediating ubiquitin E3 ligase activity that is required for its tumor suppressor function. Also forms a heterodimer with CSTF1/CSTF-50 to modulate mRNA processing and RNAP II stability by inhibiting pre-mRNA 3' cleavage.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9974R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-9974R-A680

Codice articolo locale: BOSSBS-9974R-A680

Descrizione: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15130R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-15130R-A680

Codice articolo locale: BOSSBS-15130R-A680

Descrizione: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13315R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-13315R-CY5

Codice articolo locale: BOSSBS-13315R-CY5

Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13315R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-13315R-CY7

Codice articolo locale: BOSSBS-13315R-CY7

Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15105R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-15105R-FITC

Codice articolo locale: BOSSBS-15105R-FITC

Descrizione: C20orf202 is a 122 amino acid protein that is pending further characterization. The gene encoding C20orf202 maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought to be important for seminal production and may be potential targets for male contraception.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15105R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15105R-A350

Codice articolo locale: BOSSBS-15105R-A350

Descrizione: C20orf202 is a 122 amino acid protein that is pending further characterization. The gene encoding C20orf202 maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought to be important for seminal production and may be potential targets for male contraception.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15105R-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-15105R-A647

Codice articolo locale: BOSSBS-15105R-A647

Descrizione: C20orf202 is a 122 amino acid protein that is pending further characterization. The gene encoding C20orf202 maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought to be important for seminal production and may be potential targets for male contraception.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9982R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-9982R-A680

Codice articolo locale: BOSSBS-9982R-A680

Descrizione: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13315R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-13315R-A680

Codice articolo locale: BOSSBS-13315R-A680

Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-4527R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-4527R-CY5

Codice articolo locale: BOSSBS-4527R-CY5

Descrizione: Classical swine fever(CSF) is a kind of acute and intense contagious disease in swine, it material damages swine industry. CSF could cause swine appearing disseminated hemorrhage in systemic organ and tissue, degeneration and necrosis in small vascular and capillary endothelial cells. Classical swine fever virus (CSFV) belongs to genera Pestivirus, family Flaviviridae, it’s genome total length is 12.3Kb,including a big ORF, encoding 11 structural and nonstructural proteins.Envelope glycoprotein E2 exists in the form of homodimer; this protein is cleaved from the polyprotein by a cellular signal peptidase.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15093R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15093R-A350

Codice articolo locale: BOSSBS-15093R-A350

Descrizione: C20orf134 is a 245 amino acid secreted protein that belongs to the Actin family and is encoded by a gene which maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-1982R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-1982R-A488

Codice articolo locale: BOSSBS-1982R-A488

Descrizione: MCM3 is one of the highly conserved mini-chromosome maintenance proteins that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein is a subunit of the protein complex that consists of MCM2-7. It has been shown to interact directly with MCM5/CDC46. This protein also interacts with, and thus is acetlyated by MCM3AP, a chromatin-associated acetyltransferase. The acetylation of this protein inhibits the initiation of DNA replication and cell cycle progression.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-1982R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-1982R-A350

Codice articolo locale: BOSSBS-1982R-A350

Descrizione: MCM3 is one of the highly conserved mini-chromosome maintenance proteins that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein is a subunit of the protein complex that consists of MCM2-7. It has been shown to interact directly with MCM5/CDC46. This protein also interacts with, and thus is acetlyated by MCM3AP, a chromatin-associated acetyltransferase. The acetylation of this protein inhibits the initiation of DNA replication and cell cycle progression.

UOM: 1 * 100 µl

Promo