Esta buscando: VWRA141-1444

Proveedor: Apollo Scientific

Descripción: 1,2-Cyclohexanedicarboximide 95%

Proveedor: Thermo Fisher Scientific

Descripción: 2-Fenilciclohexanona 98

FDS Certificados

Proveedor: TCI

Descripción: 1,2-Cyclohexanedicarboximide 98,0 GC, T

Numero del catalogo: (APOSOR110447-1G)

Proveedor: Apollo Scientific

Descripción: Methyl 1-methyl-1H-indole-4-carboxylate

UOM: 1 * 1 g

Promoción

Proveedor: TCI

Descripción: 2-Fenilciclohexanona 98,0 GC_ASSAY_METHOD

Numero del catalogo: (HITA810-1444)

Proveedor: VWR Collection

Descripción: PUSHING SCREW 1 * 1 UN

UOM: 1 * 1 UN

Promoción

Numero del catalogo: (SCOI285213622)

Proveedor: SI Analytics

Descripción: Valorador

UOM: 1 * 1 UN

Promoción

Proveedor: Thermo Fisher Scientific

Descripción: Cloruro de acetamidinio 97

FDS

Numero del catalogo: (H64317.06)

Proveedor: Thermo Fisher Scientific

Descripción: 1-Bromo-4-fluorobutano 97%

UOM: 1 * 5 g

Certificados Promoción

Numero del catalogo: (H56594.06)

Proveedor: Thermo Fisher Scientific

Descripción: (2-Bromoethoxy)-tert-butyldimethylsilane 98% Stabilised

UOM: 1 * 5 g

Promoción

Proveedor: Thermo Fisher Scientific

Descripción: Amonio peroxodisulfato (APS) 98

FDS Certificados

Proveedor: Thermo Fisher Scientific

Descripción: (±)-γ-Octalactona 98

FDS Certificados

Proveedor: Thermo Fisher Scientific

Descripción: Amonio peroxodisulfato (APS) ≥98.0% ACS

FDS Certificados

Proveedor: Thermo Scientific

Descripción: Designed for everyday laboratory needs the Thermo Scientific™ TSG series general purpose laboratory freezers are designed with your needs in mind. The TSG series range of freezers feature the performance, security, and quality required for your laboratory applications.

Promoción

Numero del catalogo: (BOSSBS-15344R-HRP)

Proveedor: Bioss

Descripción: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf84 gene product has been provisionally designated C9orf84 pending further characterisation. There are two isoforms of C9orf84 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-15344R-CY5)

Proveedor: Bioss

Descripción: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf84 gene product has been provisionally designated C9orf84 pending further characterisation. There are two isoforms of C9orf84 that are produced as a result of alternative splicing events.

UOM: 1 * 100 µl

Promoción