Hai cercato: genomes

Codice catalogo: (BOSSBS-13315R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-13315R-FITC

Codice articolo locale: BOSSBS-13315R-FITC

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-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-13315R-A647

Codice articolo locale: BOSSBS-13315R-A647

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-5825R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-5825R-CY3

Codice articolo locale: BOSSBS-5825R-CY3

Descrizione: The PCDHA12 gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five, which demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins which may play a role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13325R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-13325R-CY3

Codice articolo locale: BOSSBS-13325R-CY3

Descrizione: GDE4 is a 314 amino acid cytoplasmic and multi-pass membrane protein that belongs to the glycerophosphoryl diester phosphodiesterase family. Expressed in small intestine, placenta, kidney, ovary, thymus, pancreas, spleen, liver and peripheral blood leukocytes, GDE4 contains one GDPD domain and exists as three alternatively spliced isoforms. GDE4 is encoded by a gene that maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13325R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-13325R-CY5

Codice articolo locale: BOSSBS-13325R-CY5

Descrizione: GDE4 is a 314 amino acid cytoplasmic and multi-pass membrane protein that belongs to the glycerophosphoryl diester phosphodiesterase family. Expressed in small intestine, placenta, kidney, ovary, thymus, pancreas, spleen, liver and peripheral blood leukocytes, GDE4 contains one GDPD domain and exists as three alternatively spliced isoforms. GDE4 is encoded by a gene that maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-5424R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-5424R-A750

Codice articolo locale: BOSSBS-5424R-A750

Descrizione: The product of this gene functions in the NF-kappaB signal transduction pathway. The encoded protein, and the similar and functionally redundant protein MAP3K7IP2/TAB2, forms a ternary complex with the protein kinase MAP3K7/TAK1 and either TRAF2 or TRAF6 in response to stimulation with the pro-inflammatory cytokines TNF or IL-1. Subsequent MAP3K7/TAK1 kinase activity triggers a signaling cascade leading to activation of the NF-kappaB transcription factor. The human genome contains a related pseudogene. Alternatively spliced transcript variants have been described, but their biological validity has not been determined.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9979R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-9979R-A750

Codice articolo locale: BOSSBS-9979R-A750

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 C21orf70 gene product has been provisionally designated C21orf70 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15105R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-15105R-A680

Codice articolo locale: BOSSBS-15105R-A680

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-1982R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-1982R-CY7

Codice articolo locale: BOSSBS-1982R-CY7

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-15093R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-15093R-A555

Codice articolo locale: BOSSBS-15093R-A555

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: (PRSI92-289)

Fornitore: ProSci Inc.

Codice articolo fornitore: 92-289

Codice articolo locale: PRSI92-289

Descrizione: 40S ribosomal protein S7(RPS7) belongs to the S7E family of ribosomal proteins. It is phosphorylated by NEK6 during post-translational modification. RPS7 is located in the cytoplasm, binds IPO9 with high affinity. it also can interacts with NEK6. As is required for rRNA maturation and typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. The unnormal expression of RPS7 may cause Diamond-Blackfan anemia 8.

UOM: 1 * 50 µG

Promo

Codice catalogo: (BOSSBS-1982R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-1982R-A680

Codice articolo locale: BOSSBS-1982R-A680

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-9978R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-9978R-A750

Codice articolo locale: BOSSBS-9978R-A750

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 C21orf58 gene product has been provisionally designated C21orf58 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13444R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-13444R-HRP

Codice articolo locale: BOSSBS-13444R-HRP

Descrizione: GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15093R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15093R-CY3

Codice articolo locale: BOSSBS-15093R-CY3

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-15093R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-15093R-HRP

Codice articolo locale: BOSSBS-15093R-HRP

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