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Product Image-ABNOH00008995-AP51

Anti-TNFSF18 Antibody Pair

Numero del catalogo: (ABNOH00008995-AP51)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human TNFSF18.
UOM: 1 * 1 SET
Product Image-ABNOH00023396-AP51

Anti-PIP5K1C Antibody Pair

Numero del catalogo: (ABNOH00023396-AP51)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human PIP5K1C.
UOM: 1 * 1 SET
Product Image-ABNOH00055080-AP51

Anti-TAPBPL Antibody Pair

Numero del catalogo: (ABNOH00055080-AP51)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human TAPBPL.
UOM: 1 * 1 SET
Product Image-ABNOH00051564-AP11

Anti-HDAC7 Antibody Pair

Numero del catalogo: (ABNOH00051564-AP11)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human HDAC7.
UOM: 1 * 1 SET
Product Image-ABNOH00000946-AP51

Anti-SIGLEC6 Antibody Pair

Numero del catalogo: (ABNOH00000946-AP51)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human SIGLEC6.
UOM: 1 * 1 SET
Product Image-ABNOH00000203-AP14

Anti-AK1 Antibody Pair

Numero del catalogo: (ABNOH00000203-AP14)
Proveedor: Abnova
Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human AK1.
UOM: 1 * 1 SET
Product Image-ANSE37-520/9.5

Guantes de uso general, AlphaTec® 37-520

Proveedor: Ansell
Descripción: Guantes de nitrilo con forro flocado de algodón 100%.

Image Unavailable-BOSSBS-9662R-FITC

Anti-EFR3A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numero del catalogo: (BOSSBS-9662R-FITC)
Proveedor: Bioss
Descripción: EFR3A is a plasma membrane protein that contains 821 amino acids and belongs to the EFR3 family. EFR3A is alternatively spliced creating three isoforms and is encoded by a gene that maps to human chromosome 8. Human chromosome 8 consists of nearly 146 million base pairs, encodes over 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-0651R-HRP

Anti-GJA1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numero del catalogo: (BOSSBS-0651R-HRP)
Proveedor: Bioss
Descripción: Gap junction protein that acts as a regulator of bladder capacity. A gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. May play a critical role in the physiology of hearing by participating in the recycling of potassium to the cochlear endolymph. Negative regulator of bladder functional capacity: acts by enhancing intercellular electrical and chemical transmission, thus sensitizing bladder muscles to cholinergic neural stimuli and causing them to contract (By similarity).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12343R-A680

Anti-TRIB1/GIG2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-12343R-A680)
Proveedor: Bioss
Descripción: TRB-1 is a 372 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase superfamily. Expressed ubiquitously with highest expression in bone marrow, thyroid gland, skeletal muscle and pancreas, TRB-1 interacts with MAPK kinases and is thought to regulate the activation of MAP kinases, possibly controlling MAP kinase cascades. The gene encoding TRB-1 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12343R-HRP

Anti-TRIB1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numero del catalogo: (BOSSBS-12343R-HRP)
Proveedor: Bioss
Descripción: TRB-1 is a 372 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase superfamily. Expressed ubiquitously with highest expression in bone marrow, thyroid gland, skeletal muscle and pancreas, TRB-1 interacts with MAPK kinases and is thought to regulate the activation of MAP kinses, possibly controlling MAP kinase cascades. The gene encoding TRB-1 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12343R-A555

Anti-TRIB1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numero del catalogo: (BOSSBS-12343R-A555)
Proveedor: Bioss
Descripción: TRB-1 is a 372 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase superfamily. Expressed ubiquitously with highest expression in bone marrow, thyroid gland, skeletal muscle and pancreas, TRB-1 interacts with MAPK kinases and is thought to regulate the activation of MAP kinses, possibly controlling MAP kinase cascades. The gene encoding TRB-1 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12036R-FITC

Anti-HMP19 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numero del catalogo: (BOSSBS-12036R-FITC)
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-12036R-A350

Anti-HMP19 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numero del catalogo: (BOSSBS-12036R-A350)
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-12036R-CY7

Anti-HMP19 Rabbit Polyclonal Antibody (Cy7®)

Numero del catalogo: (BOSSBS-12036R-CY7)
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-12036R-A647

Anti-HMP19 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numero del catalogo: (BOSSBS-12036R-A647)
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
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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