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Image Unavailable-J62606.03

L-thyroxine 98%

Fornitore: Thermo Fisher Scientific
Descrizione: L-thyroxine 98%

MSDS Certificati

Image Unavailable-44816.14

Mercurio (II) bromuro ACS

Fornitore: Thermo Fisher Scientific
Descrizione: Mercurio (II) bromuro ACS

MSDS Certificati

Image Unavailable-BOSSBS-15262R-A350

Anti-C7ORF29 Rabbit Polyclonal Antibody (ALEXA FLUOR® 350)

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
Product Image-211-0212

VWR®, organizzatori per rack per provette per microcentrifuga

Fornitore: VWR Collection
Descrizione: Clear acrylic.

Image Unavailable-A10431.30

Caffeina ≥99%

Fornitore: Thermo Fisher Scientific
Descrizione: Caffeina ≥99%

MSDS Certificati

Image Unavailable-BOSSBS-15262R-CY7

Anti-C7ORF29 Rabbit Polyclonal Antibody (Cy7)

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
Image Unavailable-BOSSBS-15262R-A647

Anti-C7ORF29 Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

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
Image Unavailable-BOSSBS-15262R-A680

Anti-C7ORF29 Rabbit Polyclonal Antibody (ALEXA FLUOR® 680)

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
Product Image-PRSI60-034

Anti-ACER1 Rabbit Polyclonal Antibody

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


Product Image-PRSI61-865

Anti-SLC25A19 Rabbit Polyclonal Antibody

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


Image Unavailable-BOSSBS-15262R-CY3

Anti-C7ORF29 Rabbit Polyclonal Antibody (Cy3)

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
Image Unavailable-BOSSBS-15262R-A555

Anti-C7ORF29 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

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
Image Unavailable-BOSSBS-1155R-A680

Anti-ASCL1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

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
Image Unavailable-BOSSBS-15262R-HRP

Anti-C7ORF29 Rabbit Polyclonal Antibody (HRP)

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
Image Unavailable-BOSSBS-15262R-A750

Anti-C7ORF29 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

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
Image Unavailable-BOSSBS-15262R-A488

Anti-C7ORF29 Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

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
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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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Puoi ordinare questo prodotto. Se necessario, ti contatteremo per richiedere licenza, autorizzazione o dichiarazione d'uso per procedere con la fornitura.
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