Hai cercato: tert-Butyl (5-fluoro-1,3-thiazol-2-yl)carbamate

Fornitore: Thermo Fisher Scientific

Descrizione: L-thyroxine 98%

MSDS Certificati

Fornitore: Thermo Fisher Scientific

Descrizione: Mercurio (II) bromuro ACS

MSDS Certificati

Codice catalogo: (BOSSBS-15262R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-A350

Codice articolo locale: BOSSBS-15262R-A350

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Fornitore: VWR Collection

Descrizione: Clear acrylic.

Fornitore: Thermo Fisher Scientific

Descrizione: Caffeina ≥99%

MSDS Certificati

Codice catalogo: (BOSSBS-15262R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-CY7

Codice articolo locale: BOSSBS-15262R-CY7

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-A647

Codice articolo locale: BOSSBS-15262R-A647

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-A680

Codice articolo locale: BOSSBS-15262R-A680

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (PRSI60-034)

Fornitore: ProSci Inc.

Codice articolo fornitore: 60-034

Codice articolo locale: PRSI60-034

Descrizione: For WB starting dilution is: 1:1000.

UOM: 1 * 400 µl

New Product Promo

Codice catalogo: (PRSI61-865)

Fornitore: ProSci Inc.

Codice articolo fornitore: 61-865

Codice articolo locale: PRSI61-865

Descrizione: For WB starting dilution is: 1:1000.

UOM: 1 * 400 µl

New Product Promo

Codice catalogo: (BOSSBS-15262R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-CY3

Codice articolo locale: BOSSBS-15262R-CY3

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-A555

Codice articolo locale: BOSSBS-15262R-A555

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-1155R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-1155R-A680

Codice articolo locale: BOSSBS-1155R-A680

Descrizione: Transcription factor that controls transcriptional expression of its target genes by binding to the E box (5'-CANNTG-3'). Plays a role at early stages of development of specific neural lineages in most regions of the CNS, and of several lineages in the PNS. Acts synergistically with FOXN4 to specify the identity of V2b neurons rather than V2a from bipotential p2 progenitors during spinal cord neurogenesis, probably through DLL4-NOTCH signaling activation. Essential for the generation of olfactory and autonomic neurons (By similarity).

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-HRP

Codice articolo locale: BOSSBS-15262R-HRP

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-A750

Codice articolo locale: BOSSBS-15262R-A750

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-A488

Codice articolo locale: BOSSBS-15262R-A488

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo