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Image du produit-129-2921

Sacs à bouchon avec indicateur de vapeur, Tyvek® 1073B/HDPE

Fournisseur: KEYSTONE CLEANROOM PRODUCTS
Description: Les sacs pour autoclave en Tyvek® 1073B/HDPE sont idéaux pour la stérilisation à la vapeur de composants pharmaceutiques tels que les flacons, les capuchons de seringues et les bouchons. C'est également un bon choix pour les pièces d'équipement lourd où la visibilité à travers le sac est nécessaire.

Image non disponible-BOSSBS-13482R-A680

Anti-GOLGA6 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numéro de catalogue: (BOSSBS-13482R-A680)
Fournisseur: Bioss
Description: The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes.
UOM: 1 * 100 µl
Image du produit-590-0388

b.safe Entonnoirs 130

Fournisseur: Bohlender
Description: Entonnoir en PE ou PE-EX antistatique pour l'élimination des déchets liquides. L'entonnoir peut être monté en toute sécurité sur le conteneur à déchets grâce à son capuchon librement rotatif qui est fixé en toute sécurité avec le goulot de remplissage.

Image non disponible-BOSSBS-13481R-CY5

Anti-GOLGA5 Rabbit Polyclonal Antibody (Cy5®)

Numéro de catalogue: (BOSSBS-13481R-CY5)
Fournisseur: Bioss
Description: The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This protein is a coiled-coil membrane protein that has been postulated to play a role in vesicle tethering and docking. Translocations involving this gene and the ret proto-oncogene have been found in tumor tissues; the chimeric sequences have been designated RET-II and PTC5. [provided by RefSeq, Feb 2010].
UOM: 1 * 100 µl
Image non disponible-BOSSBS-11690R-CY3

Anti-FIG4/SAC3 Rabbit Polyclonal Antibody (Cy3®)

Numéro de catalogue: (BOSSBS-11690R-CY3)
Fournisseur: Bioss
Description: FIG4 is a 907 amino acid protein that contains one SAC domain through which it is thought to function as a phosphoinositide phosphatase that may play an important role in signal transduction and vesicle trafficking. Defects in the gene encoding FIG4 are the cause of Charcot-Marie-Tooth disease type 4J (CMT4J) and amyotrophic lateral sclerosis type 11 (ALS11), both of which negatively affect the nervous system. CMT4J is a recessive demyelinating disorder of the peripheral nervous system and is characterized by reduced motor nerve conduction velocities and axonal degeneration. Unlike CMT4J, ALS11 is characterized by the degeneration of upper motor neurons in the brain and lower neurons in the spinal cord, causing paralysis and, ultimately, death.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-11690R-A488

Anti-FIG4/SAC3 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numéro de catalogue: (BOSSBS-11690R-A488)
Fournisseur: Bioss
Description: FIG4 is a 907 amino acid protein that contains one SAC domain through which it is thought to function as a phosphoinositide phosphatase that may play an important role in signal transduction and vesicle trafficking. Defects in the gene encoding FIG4 are the cause of Charcot-Marie-Tooth disease type 4J (CMT4J) and amyotrophic lateral sclerosis type 11 (ALS11), both of which negatively affect the nervous system. CMT4J is a recessive demyelinating disorder of the peripheral nervous system and is characterized by reduced motor nerve conduction velocities and axonal degeneration. Unlike CMT4J, ALS11 is characterized by the degeneration of upper motor neurons in the brain and lower neurons in the spinal cord, causing paralysis and, ultimately, death.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-11690R-A647

Anti-FIG4/SAC3 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numéro de catalogue: (BOSSBS-11690R-A647)
Fournisseur: Bioss
Description: FIG4 is a 907 amino acid protein that contains one SAC domain through which it is thought to function as a phosphoinositide phosphatase that may play an important role in signal transduction and vesicle trafficking. Defects in the gene encoding FIG4 are the cause of Charcot-Marie-Tooth disease type 4J (CMT4J) and amyotrophic lateral sclerosis type 11 (ALS11), both of which negatively affect the nervous system. CMT4J is a recessive demyelinating disorder of the peripheral nervous system and is characterized by reduced motor nerve conduction velocities and axonal degeneration. Unlike CMT4J, ALS11 is characterized by the degeneration of upper motor neurons in the brain and lower neurons in the spinal cord, causing paralysis and, ultimately, death.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-3901R-CY5

Anti-CUBN Rabbit Polyclonal Antibody (Cy5®)

Numéro de catalogue: (BOSSBS-3901R-CY5)
Fournisseur: Bioss
Description: 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
Image du produit-BURK5344-8012

Sachets, SteriBag Cleanroom

Fournisseur: BURKLE
Description: Le sachet de conditionnement SteriBag Cleanroom dans un double emballage peut être directement amené dans la salle blanche. Respectivement 25 sachets se trouvent dans deux emballages qui peuvent être ouverts l’un après l’autre, idéal pour les introduire dans la salle blanche.

Image du produit-734-2953

VWR®, Single-Use Tank Liners, Medical Grade

Fournisseur: VWR Collection
Description: Ces sacs de réservoir sont des sacs à usage unique ouverts sur le haut, conçus pour s’adapter à des récipients cylindriques.

Certificats

Image non disponible-BOSSBS-11690R-A680

Anti-FIG4/SAC3 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numéro de catalogue: (BOSSBS-11690R-A680)
Fournisseur: Bioss
Description: FIG4 is a 907 amino acid protein that contains one SAC domain through which it is thought to function as a phosphoinositide phosphatase that may play an important role in signal transduction and vesicle trafficking. Defects in the gene encoding FIG4 are the cause of Charcot-Marie-Tooth disease type 4J (CMT4J) and amyotrophic lateral sclerosis type 11 (ALS11), both of which negatively affect the nervous system. CMT4J is a recessive demyelinating disorder of the peripheral nervous system and is characterised by reduced motor nerve conduction velocities and axonal degeneration. Unlike CMT4J, ALS11 is characterised by the degeneration of upper motor neurons in the brain and lower neurons in the spinal cord, causing paralysis and, ultimately, death.
UOM: 1 * 100 µl
Image non disponible-SARBYWCG02

Accessories for safety weighing cabinets SWC series

Numéro de catalogue: (SARBYWCG02)
Fournisseur: Sartorius Balances
Description: Sac pour trémie jetable, Pour: Hottes de pesée de sécurité, série SWC
UOM: 1 * 50 ST
Image non disponible-BOSSBS-13482R-CY5

Anti-GOLGA6 Rabbit Polyclonal Antibody (Cy5®)

Numéro de catalogue: (BOSSBS-13482R-CY5)
Fournisseur: Bioss
Description: The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-3901R-A680

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

Numéro de catalogue: (BOSSBS-3901R-A680)
Fournisseur: Bioss
Description: 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-foetal interface.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13482R-FITC

Anti-GOLGA6 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numéro de catalogue: (BOSSBS-13482R-FITC)
Fournisseur: Bioss
Description: The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-11690R-A555

Anti-FIG4/SAC3 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-11690R-A555)
Fournisseur: Bioss
Description: FIG4 is a 907 amino acid protein that contains one SAC domain through which it is thought to function as a phosphoinositide phosphatase that may play an important role in signal transduction and vesicle trafficking. Defects in the gene encoding FIG4 are the cause of Charcot-Marie-Tooth disease type 4J (CMT4J) and amyotrophic lateral sclerosis type 11 (ALS11), both of which negatively affect the nervous system. CMT4J is a recessive demyelinating disorder of the peripheral nervous system and is characterized by reduced motor nerve conduction velocities and axonal degeneration. Unlike CMT4J, ALS11 is characterized by the degeneration of upper motor neurons in the brain and lower neurons in the spinal cord, causing paralysis and, ultimately, death.
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 016 385 011
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