Esta buscando: 2,3,6-Trifluorobenzaldeh\\u00EDdo

Proveedor: Thermo Fisher Scientific

Descripción: L(+)-Asparraguina, anhidro 99%

FDS Certificados

Proveedor: Thermo Fisher Scientific

Descripción: Cafeína ≥99%

FDS Certificados

Proveedor: Thermo Fisher Scientific

Descripción: Dibromuro de mercurio ACS

FDS Certificados

Numero del catalogo: (BOSSBS-15262R-A350)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-15262R-CY3)

Proveedor: Bioss

Descripción: 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

Promoción

Proveedor: Thermo Fisher Scientific

Descripción: Ácido nicotínico (Niacin) ≥99%

FDS Certificados

Numero del catalogo: (BOSSBS-15262R-CY7)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-15262R-A647)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-15262R-A680)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (PRSI61-865)

Proveedor: ProSci Inc.

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

UOM: 1 * 400 µl

New Product Promoción

Numero del catalogo: (PRSI60-394)

Proveedor: ProSci Inc.

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

UOM: 1 * 400 µl

New Product Promoción

Numero del catalogo: (PRSI60-034)

Proveedor: ProSci Inc.

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

UOM: 1 * 400 µl

New Product Promoción

Numero del catalogo: (BOSSBS-15262R-A750)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-15262R-HRP)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-15262R-A488)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-1155R-A750)

Proveedor: Bioss

Descripción: 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

Promoción