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Image Unavailable-BOSSBS-8211R-CY5.5

Anti-FAM84B Rabbit Polyclonal Antibody (Cy5.5®)

Numero del catalogo: (BOSSBS-8211R-CY5.5)
Proveedor: Bioss
Descripción: FAM84B, also known as NSE2 or BCMP101, is a 310 amino acid protein that is expressed in esophageal squamous cell carcinomas, suggesting a role in tumor development and metastasis. The gene encoding FAM84B maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8211R-A750

Anti-BCMP101 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numero del catalogo: (BOSSBS-8211R-A750)
Proveedor: Bioss
Descripción: FAM84B, also known as NSE2 or BCMP101, is a 310 amino acid protein that is expressed in esophageal squamous cell carcinomas, suggesting a role in tumor development and metastasis. The gene encoding FAM84B maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12036R

Anti-HMP19 Rabbit Polyclonal Antibody

Numero del catalogo: (BOSSBS-12036R)
Proveedor: Bioss
Descripción: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15130R-CY7

Anti-C21orf88 Rabbit Polyclonal Antibody (Cy7®)

Numero del catalogo: (BOSSBS-15130R-CY7)
Proveedor: Bioss
Descripción: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8542R-CY7

Anti-MSH3 Rabbit Polyclonal Antibody (Cy7®)

Numero del catalogo: (BOSSBS-8542R-CY7)
Proveedor: Bioss
Descripción: Component of the post-replicative DNA mismatch repair system (MMR). Heterodimerizes with MSH2 to form MutS beta which binds to DNA mismatches thereby initiating DNA repair. When bound, the MutS beta heterodimer bends the DNA helix and shields approximately 20 base pairs. MutS beta recognizes large insertion-deletion loops (IDL) up to 13 nucleotides long. After mismatch binding, forms a ternary complex with the MutL alpha heterodimer, which is thought to be responsible for directing the downstream MMR events, including strand discrimination, excision, and resynthesis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15130R-A555

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numero del catalogo: (BOSSBS-15130R-A555)
Proveedor: Bioss
Descripción: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15130R-A647

Anti-C21orf88 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numero del catalogo: (BOSSBS-15130R-A647)
Proveedor: Bioss
Descripción: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9976R-A680

Anti-C21orf128 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-9976R-A680)
Proveedor: Bioss
Descripción: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf128 gene product has been provisionally designated C21orf128 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9975R-A750

Anti-C21ORF62 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numero del catalogo: (BOSSBS-9975R-A750)
Proveedor: Bioss
Descripción: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterisation.
UOM: 1 * 100 µl
Product Image-ABNOH00003224-AP21

Anti-HOXC8 Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00003224-AP21)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human HOXC8.
UOM: 1 * 1 SET
Product Image-ABNOH00002288-AP21

Anti-FKBP4 Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00002288-AP21)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human FKBP4.
UOM: 1 * 1 SET
Product Image-ABNOH00005831-AP21

Anti-PYCR1 Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00005831-AP21)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human PYCR1.
UOM: 1 * 1 SET
Product Image-ABNOH00005957-AP21

Anti-RCVRN Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00005957-AP21)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human RCVRN.
UOM: 1 * 1 SET
Product Image-ABNOH00005917-AP22

Anti-RARS Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00005917-AP22)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human RARS.
UOM: 1 * 1 SET
Product Image-ABNOH00000191-AP21

Anti-AHCY Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00000191-AP21)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human AHCY.
UOM: 1 * 1 SET
Product Image-ABNOH00051564-AP21

Anti-HDAC7 Polyclonal Antibody Pair

Numero del catalogo: (ABNOH00051564-AP21)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human HDAC7.
UOM: 1 * 1 SET
Consulta de precio
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta. Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta.
Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto ha sido bloqueado por su organización. Por favor, pónganse en contacto con su departamento de compras para obtener más información.
El producto original ya no está disponible. Su sustituto se muestra a continuación.
El producto(s) marcados con este símbolo están descatalogados - se venden hasta acabar stock. Pueden encontrar alternativas buscando con el número de catálogo VWR listado arriba. Si necesita más ayuda, por favor llame al Servicio de atención al cliente de VWR al 902.222.897.
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