You Searched For: 2,3,6-Trimethylphenol

Supplier: Thermo Fisher Scientific

Description: (2S,4S)-4-Fluoropyrrolidine-2-carboxamide hydrochloride 98%

MSDS Certificates

Supplier: Thermo Fisher Scientific

Description: L(+)-Asparagine, anhydrous 99%

MSDS Certificates

Supplier: Thermo Fisher Scientific

Description: Caprylic acid ≥98%

MSDS Certificates

Supplier: Thermo Fisher Scientific

Description: 4-Chloro-m-cresol ≥99%

MSDS Certificates

Supplier: Thermo Fisher Scientific

Description: (S)-(-)-2,2'-Diamino-1,1'-binaphthalene 97%

MSDS

Supplier: Thermo Fisher Scientific

Description: L-thyroxine 98%

MSDS Certificates

Supplier: Thermo Fisher Scientific

Description: Mercury(II) bromide ACS

MSDS Certificates

Supplier: Thermo Fisher Scientific

Description: (1-Propyl)triphenylphosphonium bromide ≥99%

MSDS Certificates

Catalog Number: (BOSSBS-15262R-A680)

Supplier: Bioss

Description: 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

Sale

Catalog Number: (BOSSBS-15262R-CY7)

Supplier: Bioss

Description: 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

Sale

Catalog Number: (BOSSBS-15262R-A647)

Supplier: Bioss

Description: 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

Sale

Catalog Number: (BOSSBS-15262R-CY3)

Supplier: Bioss

Description: 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

Sale

Supplier: VWR Collection

Description: Clear acrylic.

Catalog Number: (BOSSBS-15262R-HRP)

Supplier: Bioss

Description: 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

Sale

Catalog Number: (BOSSBS-15262R-A750)

Supplier: Bioss

Description: 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

Sale

Catalog Number: (BOSSBS-15262R-A555)

Supplier: Bioss

Description: 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

Sale