Imprimir…

Esta buscando: Frascos de lavado


146 844  results were found

Refinar resultados Ordenado por
SearchResultCount:"146844"

Sort Results

Vista lista Vista Extendida (Nueva)

Valore los resultados de su búsqueda

Product Image-REST20600

High-capacity oxygen trap

Proveedor: Restek
Descripción: These high-capacity oxygen trap removes up to 135 ml of oxygen or 2 g of water.

Product Image-231-2001

Cucharas de medición

Numero del catalogo: (231-2001)
Proveedor: VITLAB
Descripción: PP, blanco. Con extremos planos achaflanados y asa reforzada.
UOM: 1 * 12 UN
Product Image-634-8590

Cells and accessories for Lovibond® Comparator 2000+

Numero del catalogo: (634-8590)
Proveedor: Lovibond
Descripción: Cubetas de cristal cuadradas DB424/S, longitud de trayectoria de 13,5 mm, con tapa, Para: Comparator 2000+ systems
UOM: 1 * 5 UN
Product Image-HEAT120661

Mini LED light box

Numero del catalogo: (HEAT120661)
Proveedor: HEATHROW
Descripción: This small light box saves bench space and can be stored in a drawer.
UOM: 1 * 1 UN
Product Image-410-9132

Manos

Numero del catalogo: (410-9132)
Proveedor: MORGAN ADVANCED MATERIALS HALD
Descripción: Porcelana con mango vidriado, superficie de molienda no vidriada.
UOM: 1 * 1 UN
Image Unavailable-BOSSBS-9932R-A680

Anti-C11ORF46 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-9932R-A680)
Proveedor: Bioss
Descripción: C11orf46, also known as FLJ38968 or dJ299F11.1, is a 260 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12479R-A488

Anti-ANO3 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numero del catalogo: (BOSSBS-12479R-A488)
Proveedor: Bioss
Descripción: TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
UOM: 1 * 100 µl
Product Image-ENDRCPS31E-1020/0

Memosens pH Sensors for Disinfection, CPS31E

Proveedor: Endress+Hauser
Descripción: pH sensor for application in drinking water and swimming pools.

New Product

Image Unavailable-BOSSBS-9941R-A680

Anti-C11orf71 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-9941R-A680)
Proveedor: Bioss
Descripción: C11orf71, also known as FLJ20010, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9939R-A680

Anti-C11orf57 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-9939R-A680)
Proveedor: Bioss
Descripción: C11orf57, also known as FLJ10726, is a 292 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9898R-A750

Anti-GI24 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numero del catalogo: (BOSSBS-9898R-A750)
Proveedor: Bioss
Descripción: Platelet receptor GI24, also known as SISP1 or PP2135, is a 311 amino acid single-pass type I membrane protein that contains one Ig-like (immunoglobulin-like) domain. GI24 is thought to contribute to tumour-invasive growth in the collagen matrix and is encoded by a gene that maps to human chromosome 10q22.1. Chromosome 10 contains over 800 genes, 135 million nucleotides and comprises nearly 4.5% of the human genome. PTEN is an important tumour suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterised by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11888R-CY5

Anti-MPPED2 Rabbit Polyclonal Antibody (Cy5®)

Numero del catalogo: (BOSSBS-11888R-CY5)
Proveedor: Bioss
Descripción: MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double stranded DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
UOM: 1 * 100 µl
Product Image-SCOI285103553

Platinum electrode, ScienceLine

Numero del catalogo: (SCOI285103553)
Proveedor: SI Analytics
Descripción: Single platinum electrode, with glass shaft and ring shaped sensor (Ø 6 mm). For titration purposes.
UOM: 1 * 1 UN
Product Image-BAND3053

Accessories for SONOREX ultrasonic baths

Numero del catalogo: (BAND3053)
Proveedor: BANDELIN-ELECTRONIC
Descripción: Ultrasonic bath accessories, Insert tub, KW 10-0, plastic with cap, dimensions 242×182×135 mm, Para: SUPER RK 510 / H, DIGITEC DT 510 H / H-RC
UOM: 1 * 1 UN
Image Unavailable-CORAG179521

General purpose trays

Numero del catalogo: (CORAG179521)
Proveedor: Gilac PROFESSIONNEL
Descripción: Trays, made of HDPE, ideal for lifting the dough and used for storage purpose.
UOM: 1 * 1 UN
Product Image-VARI6610021100

Micro cuvettes

Numero del catalogo: (VARI6610021100)
Proveedor: VARIAN
Descripción: Black walled rectangular UV quartz cuvettes self masking to match the Cary 50 specifications.
UOM: 1 * 1 UN
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.
497 - 512 of 146 844
no targeter for Bottom