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Proveedor: Whatman products (Cytiva)
Descripción: MBS I is an excellent system for optimal microbiological control using membranes. The overall procedure time is reduced to a minimum. The design of the system, which consists of an electrical membrane dispenser, a funnel dispenser, and a vacuum manifold, leads to more reproducible results. All components are sold separately. The modular system provides flexibility to select the hardware and accessories that best suit the unique and varied workflows of the user.
The special sealing technique ensures easy handling and high integrity of the funnel and membrane during filtration. This keeps any cross-contamination to a minimum.

Numero del catalogo: (BOSSBS-9006R)
Proveedor: Bioss
Descripción: Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.
UOM: 1 * 100 µl


Numero del catalogo: (ANTIA314822-100)
Proveedor: ANTIBODIES.COM
Descripción: Recombinant rabbit monoclonal [CKBB/8608R] antibody to Creatine Kinase MB for IHC-P with samples derived from human.
UOM: 1 * 100 µG

New Product


Numero del catalogo: (ANTIA316204-100)
Proveedor: ANTIBODIES.COM
Descripción: Recombinant mouse monoclonal [rCKBB/8842] antibody to creatine kinase MB for IHC-P with samples derived from human.
UOM: 1 * 100 µG

New Product


Numero del catalogo: (ANTIA314815-100)
Proveedor: ANTIBODIES.COM
Descripción: Mouse monoclonal [CKBB/6565] antibody to Creatine Kinase MB for ELISA, WB and IHC-P with samples derived from human.
UOM: 1 * 100 µG

New Product


Numero del catalogo: (ANTIA314816-100)
Proveedor: ANTIBODIES.COM
Descripción: Mouse monoclonal [CKBB/6566] antibody to Creatine Kinase MB for ELISA, WB and IHC-P with samples derived from human.
UOM: 1 * 100 µG

New Product


Numero del catalogo: (BOSSBS-3901R-A488)
Proveedor: Bioss
Descripción: Cotransporter which plays a role in lipoprotein, vitamin and iron metabolism, by facilitating their uptake. Binds to ALB, MB, Kappa and lambda-light chains, TF, hemoglobin, GC, SCGB1A1, APOA1, high density lipoprotein, and the GIF-cobalamin complex. The binding of all ligands requires calcium. Serves as important transporter in several absorptive epithelia, including intestine, renal proximal tubules and embryonic yolk sac. Interaction with LRP2 mediates its trafficking throughout vesicles and facilitates the uptake of specific ligands like GC, hemoglobin, ALB, TF and SCGB1A1. Interaction with AMN controls its trafficking to the plasma membrane and facilitates endocytosis of ligands. May play an important role in the development of the peri-implantation embryo through internalization of APOA1 and cholesterol. Binds to LGALS3 at the maternal-fetal interface.
UOM: 1 * 100 µl


Numero del catalogo: (ABNOMAB1992)
Proveedor: Abnova
Descripción: Mouse monoclonal antibody raised against partial recombinant MSLN.
UOM: 1 * 100 µl


Proveedor: Thermo Fisher Scientific
Descripción: Micro BCA™ protein assay kit is a specialised version of Pierce™ BCA protein assay for determining the protein concentration of dilute samples.

Proveedor: OHAUS
Descripción: Proporciona resultados precisos y reproducibles con una legibilidad del 0,1% o del 0,05%.

Numero del catalogo: (630-1830)
Proveedor: MOTIC
Descripción: Accessory for microscopes, Para: BA 210 Elite/BA310 Elite, Accesorio de fluorescencia EPI-LED con cubo de filtrado MB estándar y módulo LED de 470 nm
UOM: 1 * 1 UN


Numero del catalogo: (ABNOMAB14282)
Proveedor: Abnova
Descripción: Mouse monoclonal antibody raised against native human HLA-DRA.
UOM: 1 * 100 µG


Numero del catalogo: (BOSSBS-9006R-A488)
Proveedor: Bioss
Descripción: Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-9006R-A555)
Proveedor: Bioss
Descripción: Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.
UOM: 1 * 100 µl


Numero del catalogo: (AATB833)
Proveedor: AAT BIOQUEST
Descripción: Methylene Blue (MB) is widely used as a redox indicator in nucleic acid research.
UOM: 1 * 1 mg

New Product


Numero del catalogo: (BOSSBS-9006R-A350)
Proveedor: Bioss
Descripción: Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.
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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