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Image Unavailable-634-0799

Accessoires

Référence Produit: (634-0799)
Fournisseur: VWR Collection
Description: Accessoire pour spectrophotomètre UV/Vis, Porte-cuve avec circulation d'eau, avec agitateurs magnétiques pour agitation de la solution échantillon, Pour: U-5300
UOM: 1 * 1 Pce
Product Image-705-1099

VWR®, Accessories for Pocket Colorimeters, MCP 100 and MCT 100

Fournisseur: VWR Collection
Description: Colorimètre, Tige d'agitation en plastique

Product Image-211-8040

Supports de microtubes pour bains-marie

Référence Produit: (211-8040)
Fournisseur: SCHAEFER GUENTHER KUNSTSTOF
Description: Plastique acrylique transparent
UOM: 1 * 1 Pce
Image Unavailable-BOSSBS-8360R-CY3

Anti-LRRC2 Rabbit Polyclonal Antibody (Cy3®)

Référence Produit: (BOSSBS-8360R-CY3)
Fournisseur: Bioss
Description: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8360R-CY5.5

Anti-LRRC2 Rabbit Polyclonal Antibody (Cy5.5®)

Référence Produit: (BOSSBS-8360R-CY5.5)
Fournisseur: Bioss
Description: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM: 1 * 100 µl
Product Image-MILFYT310RAHW

Rotary Agitator

Référence Produit: (MILFYT310RAHW)
Fournisseur: Merck
Description: If your waste samples contain non-volatile or semi-volatile substances or metals, use this hazardous waste filtration system for saparation, extratction, and filtration.
UOM: 1 * 1 Pce
Image Unavailable-BOSSBS-8360R

Anti-LRRC2 Rabbit Polyclonal Antibody

Référence Produit: (BOSSBS-8360R)
Fournisseur: Bioss
Description: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8360R-A647

Anti-LRRC2 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Référence Produit: (BOSSBS-8360R-A647)
Fournisseur: Bioss
Description: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0235R-CY7

Anti-PMP22 Rabbit Polyclonal Antibody (Cy7®)

Référence Produit: (BOSSBS-0235R-CY7)
Fournisseur: Bioss
Description: PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15452R

Anti-HEMK1 Rabbit Polyclonal Antibody

Référence Produit: (BOSSBS-15452R)
Fournisseur: Bioss
Description: HEMK1 is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. name change
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8319R

Anti-HDHD2B Rabbit Polyclonal Antibody

Référence Produit: (BOSSBS-8319R)
Fournisseur: Bioss
Description: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8360R-HRP

Anti-LRRC2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Référence Produit: (BOSSBS-8360R-HRP)
Fournisseur: Bioss
Description: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0235R-A647

Anti-PMP22 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Référence Produit: (BOSSBS-0235R-A647)
Fournisseur: Bioss
Description: PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0235R-CY5.5

Anti-PMP22 Rabbit Polyclonal Antibody (Cy5.5®)

Référence Produit: (BOSSBS-0235R-CY5.5)
Fournisseur: Bioss
Description: PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15452R-HRP

Anti-HEMK1 Rabbit Polyclonal Antibody (HRP)

Référence Produit: (BOSSBS-15452R-HRP)
Fournisseur: Bioss
Description: HEMK1 is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3 name change.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8360R-FITC

Anti-LRRC2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Référence Produit: (BOSSBS-8360R-FITC)
Fournisseur: Bioss
Description: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM: 1 * 100 µl
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Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l'call est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 01 45 14 89 12.
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Veuillez noter qu'une autorisation peut être nécessaire pour commander ce produit. Un représentant de VWR vous contactera si votre commande le nécessite.
Ce produit a été bloqué par votre entreprise. Veuillez s'il vous plait contacter votre service achats pour plus d'informations.
Le produit original n'est plus disponible. Le remplacement représenté est disponible
Ce produit n'est plus disponible. Des alternatives peuvent être disponibles en faisant une recherche avec la référence VWR ci-dessus. Si vous avez besoin d'aide, s'il vous plaît appelez le Service Clients au 0825 02 30 30 (0,18 € TTC/mn).
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