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Product Image-SCOT286041803

Stopcock keys, hollow, DURAN®

Descrizione: DURAN®, borosilicate glass 3.3, clear.
Codice catalogo: SCOT286041803
UOM: 1 * 1 pezzi
Codice articolo fornitore: 286041803
Codice articolo locale: SCOT286041803
Fornitore: DWK Life Sciences
Product Image-SCOR1026993

Glass tubings, DURAN® borosilicate glass

Descrizione: Borosilicate glass acc. to ISO 3585, all-purpose glass for apparatus for the chemical industry, for pipelines and laboratory.
Codice catalogo: SCOR1026993
UOM: 1 * 16,6 kg
Codice articolo fornitore: 1026993
Codice articolo locale: SCOR1026993
Fornitore: Schott AG
Image Unavailable-BOSSBS-15073R

Anti-C1orf64 Rabbit Polyclonal Antibody

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.
Codice catalogo: BOSSBS-15073R
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15073R
Codice articolo locale: BOSSBS-15073R
Fornitore: Bioss
Image Unavailable-BOSSBS-6643R-A750

Anti-SCYL1BP1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

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 characterised 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.
Codice catalogo: BOSSBS-6643R-A750
UOM: 1 * 100 µl
Codice articolo fornitore: BS-6643R-A750
Codice articolo locale: BOSSBS-6643R-A750
Fornitore: Bioss
Image Unavailable-BOSSBS-1548R-A350

Anti-FOXO3A Rabbit Polyclonal Antibody (Alexa Fluor® 350)

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.
Codice catalogo: BOSSBS-1548R-A350
UOM: 1 * 100 µl
Codice articolo fornitore: BS-1548R-A350
Codice articolo locale: BOSSBS-1548R-A350
Fornitore: Bioss
Image Unavailable-BOSSBS-10283R-CY3

Anti-PHB2 Rabbit Polyclonal Antibody (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.
Codice catalogo: BOSSBS-10283R-CY3
UOM: 1 * 100 µl
Codice articolo fornitore: BS-10283R-CY3
Codice articolo locale: BOSSBS-10283R-CY3
Fornitore: Bioss
Image Unavailable-BOSSBS-15066R-A647

Anti-C1orf43 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descrizione: C1orf43, also known as Hepatitis C virus NS5A-transactivated protein 4 and Protein NICE-3, is a 253 amino acid single-pass membrane protein. There are five isoforms of C1orf43 that are produced as a result of alternative splicing events. The gene encoding C1orf43 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.
Codice catalogo: BOSSBS-15066R-A647
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15066R-A647
Codice articolo locale: BOSSBS-15066R-A647
Fornitore: Bioss
Image Unavailable-BOSSBS-15066R-HRP

Anti-C1orf43 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Descrizione: C1orf43, also known as Hepatitis C virus NS5A-transactivated protein 4 and Protein NICE-3, is a 253 amino acid single-pass membrane protein. There are five isoforms of C1orf43 that are produced as a result of alternative splicing events. The gene encoding C1orf43 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.
Codice catalogo: BOSSBS-15066R-HRP
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15066R-HRP
Codice articolo locale: BOSSBS-15066R-HRP
Fornitore: Bioss
Image Unavailable-BOSSBS-15018R-CY3

Anti-C1orf131 Rabbit Polyclonal Antibody (Cy3®)

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 C1orf131 gene product has been provisionally designated C1orf131 pending further characterization.
Codice catalogo: BOSSBS-15018R-CY3
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15018R-CY3
Codice articolo locale: BOSSBS-15018R-CY3
Fornitore: Bioss
Image Unavailable-BOSSBS-15043R-CY3

Anti-C1orf182 Rabbit Polyclonal Antibody (Cy3®)

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 C1orf182 gene product has been provisionally designated C1orf182 pending further characterization.
Codice catalogo: BOSSBS-15043R-CY3
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15043R-CY3
Codice articolo locale: BOSSBS-15043R-CY3
Fornitore: Bioss
Image Unavailable-BOSSBS-15037R-CY5

Anti-C1orf172 Rabbit Polyclonal Antibody (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 C1orf172 gene product has been provisionally designated C1orf172 pending further characterization.
Codice catalogo: BOSSBS-15037R-CY5
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15037R-CY5
Codice articolo locale: BOSSBS-15037R-CY5
Fornitore: Bioss
Image Unavailable-BOSSBS-15048R-CY7

Anti-C1orf189 Rabbit Polyclonal Antibody (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 C1orf189 gene product has been provisionally designated C1orf189 pending further characterization.
Codice catalogo: BOSSBS-15048R-CY7
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15048R-CY7
Codice articolo locale: BOSSBS-15048R-CY7
Fornitore: Bioss
Image Unavailable-BOSSBS-15011R-CY7

Anti-C1orf122 Rabbit Polyclonal Antibody (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 C1orf122 gene product has been provisionally designated C1orf122 pending further characterization.
Codice catalogo: BOSSBS-15011R-CY7
UOM: 1 * 100 µl
Codice articolo fornitore: BS-15011R-CY7
Codice articolo locale: BOSSBS-15011R-CY7
Fornitore: Bioss
Image Unavailable-BOSSBS-0519R-A647

Anti-ATF3 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descrizione: This protein binds the cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), a sequence present in many viral and cellular promoters. Represses transcription from promoters with ATF sites. It may repress transcription by stabilizing the binding of inhibitory cofactors at the promoter. Isoform 2 activates transcription presumably by sequestering inhibitory cofactors away from the promoters.
Codice catalogo: BOSSBS-0519R-A647
UOM: 1 * 100 µl
Codice articolo fornitore: BS-0519R-A647
Codice articolo locale: BOSSBS-0519R-A647
Fornitore: Bioss
Image Unavailable-BOSSBS-0519R-CY7

Anti-ATF3 Rabbit Polyclonal Antibody (Cy7®)

Descrizione: This protein binds the cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), a sequence present in many viral and cellular promoters. Represses transcription from promoters with ATF sites. It may repress transcription by stabilizing the binding of inhibitory cofactors at the promoter. Isoform 2 activates transcription presumably by sequestering inhibitory cofactors away from the promoters.
Codice catalogo: BOSSBS-0519R-CY7
UOM: 1 * 100 µl
Codice articolo fornitore: BS-0519R-CY7
Codice articolo locale: BOSSBS-0519R-CY7
Fornitore: Bioss
Image Unavailable-BOSSBS-0519R-A750

Anti-ATF3 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descrizione: This protein binds the cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), a sequence present in many viral and cellular promoters. Represses transcription from promoters with ATF sites. It may repress transcription by stabilizing the binding of inhibitory cofactors at the promoter. Isoform 2 activates transcription presumably by sequestering inhibitory cofactors away from the promoters.
Codice catalogo: BOSSBS-0519R-A750
UOM: 1 * 100 µl
Codice articolo fornitore: BS-0519R-A750
Codice articolo locale: BOSSBS-0519R-A750
Fornitore: Bioss
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