Hai cercato: Tyrphostin+AG+835

Codice catalogo: (BOSSBS-1548R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-1548R-CY7

Codice articolo locale: BOSSBS-1548R-CY7

Descrizione: Transcriptional activator which triggers apoptosis in the absence of survival factors, including neuronal cell death upon oxidative stress. recognises and binds to the DNA sequence 5'-[AG]TAAA[TC]A-3'. Participates in post-transcriptional regulation of MYC: following phosphorylation by MAPKAPK5, promotes induction of miR-34b and miR-34C expression, 2 post-transcriptional regulators of MYC that bind to the 3'UTR of MYC transcript and prevent its translation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-1548R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-1548R-CY3

Codice articolo locale: BOSSBS-1548R-CY3

Descrizione: Transcriptional activator which triggers apoptosis in the absence of survival factors, including neuronal cell death upon oxidative stress. recognises and binds to the DNA sequence 5'-[AG]TAAA[TC]A-3'. Participates in post-transcriptional regulation of MYC: following phosphorylation by MAPKAPK5, promotes induction of miR-34b and miR-34C expression, 2 post-transcriptional regulators of MYC that bind to the 3'UTR of MYC transcript and prevent its translation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15073R)

Fornitore: Bioss

Codice articolo fornitore: BS-15073R

Codice articolo locale: BOSSBS-15073R

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf64 gene product has been provisionally designated C1orf64 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (JULA9021709.D)

Fornitore: Julabo GmbH

Codice articolo fornitore: 9021709.D

Codice articolo locale: JULA9021709.D

Descrizione: The JULABO beer forcing test bath in conjunction with a photometer determines the product life of beer before clouding. The simulated aging process is achieved through a programmable temperature profile, which is repeated, until the first clouding develops.

UOM: 1 * 1 pezzi

Promo

Codice catalogo: (BOSSBS-10283R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-10283R-CY3

Codice articolo locale: BOSSBS-10283R-CY3

Descrizione: Acts as a mediator of transcriptional repression by nuclear hormone receptors via recruitment of histone deacetylases (By similarity). Functions as an estrogen receptor (ER)-selective coregulator that potentiates the inhibitory activities of antiestrogens and represses the activity of estrogens. Competes with NCOA1 for modulation of ER transcriptional activity. Probably involved in regulating mitochondrial respiration activity and in aging.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-6643R)

Fornitore: Bioss

Codice articolo fornitore: BS-6643R

Codice articolo locale: BOSSBS-6643R

Descrizione: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-10283R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-10283R-A350

Codice articolo locale: BOSSBS-10283R-A350

Descrizione: Acts as a mediator of transcriptional repression by nuclear hormone receptors via recruitment of histone deacetylases (By similarity). Functions as an estrogen receptor (ER)-selective coregulator that potentiates the inhibitory activities of antiestrogens and represses the activity of estrogens. Competes with NCOA1 for modulation of ER transcriptional activity. Probably involved in regulating mitochondrial respiration activity and in aging.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-10283R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-10283R-A750

Codice articolo locale: BOSSBS-10283R-A750

Descrizione: Acts as a mediator of transcriptional repression by nuclear hormone receptors via recruitment of histone deacetylases (By similarity). Functions as an estrogen receptor (ER)-selective coregulator that potentiates the inhibitory activities of antiestrogens and represses the activity of estrogens. Competes with NCOA1 for modulation of ER transcriptional activity. Probably involved in regulating mitochondrial respiration activity and in aging.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-3140R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-3140R-CY7

Codice articolo locale: BOSSBS-3140R-CY7

Descrizione: Transcriptional activator which triggers apoptosis in the absence of survival factors, including neuronal cell death upon oxidative stress. Recognizes and binds to the DNA sequence 5'-[AG]TAAA[TC]A-3'. Participates in post-transcriptional regulation of MYC: following phosphorylation by MAPKAPK5, promotes induction of miR-34b and miR-34c expression, 2 post-transcriptional regulators of MYC that bind to the 3'UTR of MYC transcript and prevent its translation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (50484-100ML-F)

Fornitore: SIGMA ALDRICH MICROSCOPY

Codice articolo fornitore: 50484-100ML-F

Codice articolo locale: SIAM50484-100ML-F

Descrizione: Ehrlich’s reagent III, Loeffler’s Methylene Blue. Methylene Blue was earlier recognized as a good nuclear stain, the staining solutions are always either aged or alkalized, if not both. More importantly it is an excellent stain for ribonucleic acid, which is the important stainable constituent of bacterial bodies, of lymphocyte and hemoportoal cytoplasm, and of nerve cell tigroid granules. It can also be employed in capsule stain. The capsule stain begins as a negative stain leaving the organisms colorless. The capsule are clearly seen as halo surrounding the bacterial cell. Another staining procedure is performed with nigrosin (Cat. No. 43925).

UOM: 1 * 100 mL

Promo

Codice catalogo: (BOSSBS-15078R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15078R-CY7

Codice articolo locale: BOSSBS-15078R-CY7

Descrizione: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15035R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-15035R-A555

Codice articolo locale: BOSSBS-15035R-A555

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf168 gene product has been provisionally designated C1orf168 pending further characterization. There are two isoforms of C1orf168 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15035R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-15035R-A750

Codice articolo locale: BOSSBS-15035R-A750

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf168 gene product has been provisionally designated C1orf168 pending further characterization. There are two isoforms of C1orf168 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15044R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-15044R-CY5

Codice articolo locale: BOSSBS-15044R-CY5

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf183 gene product has been provisionally designated C1orf183 pending further characterization. There are two isoforms of C1orf183 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15040R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15040R-CY7

Codice articolo locale: BOSSBS-15040R-CY7

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf177 gene product has been provisionally designated C1orf177 pending further characterization. There are two isoforms of C1orf177 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15080R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-15080R-HRP

Codice articolo locale: BOSSBS-15080R-HRP

Descrizione: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf87 gene product has been provisionally designated C1orf87 pending further characterization. There are three isoforms of C1orf87 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promo