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Image Unavailable-BOSSBS-11060R-A750

Anti-OTOA/DFNB22 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalogus nummer: (BOSSBS-11060R-A750)
Leverancier: Bioss
Omschrijving: Otoancorin, also known as OTOA, CT108 or DFNB22, is a 1153 amino acid protein belonging to the stereocilin family. Expressed in the inner ear and restricted to the interface between the apical surface of sensory epithelia, otoancorin is suggested to act as an adhesion molecule. Otoancorin ensures the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in the gene encoding otoancorin leads to deafness autosomal recessive type 22 (DFNB22), which is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain or the area of the brain that receives sound information. Existing as three alternatively spliced isoforms, otoancorin is encoded by a gene located on human chromosome 16p12.2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-4065R-HRP

Anti-P2RX2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalogus nummer: (BOSSBS-4065R-HRP)
Leverancier: Bioss
Omschrijving: Ion channel gated by extracellular ATP involved in a variety of cellular responses, such as excitatory postsynaptic responses in sensory neurons, neuromuscular junctions (NMJ) formation, hearing, perception of taste and peristalsis. In the inner ear, regulates sound transduction and auditory neurotransmission, outer hair cell electromotility, inner ear gap junctions, and K(+) recycling. Mediates synaptic transmission between neurons and from neurons to smooth muscle.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-4065R-A488

Anti-P2RX2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalogus nummer: (BOSSBS-4065R-A488)
Leverancier: Bioss
Omschrijving: Ion channel gated by extracellular ATP involved in a variety of cellular responses, such as excitatory postsynaptic responses in sensory neurons, neuromuscular junctions (NMJ) formation, hearing, perception of taste and peristalsis. In the inner ear, regulates sound transduction and auditory neurotransmission, outer hair cell electromotility, inner ear gap junctions, and K(+) recycling. Mediates synaptic transmission between neurons and from neurons to smooth muscle.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-4065R-A350

Anti-P2RX2 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalogus nummer: (BOSSBS-4065R-A350)
Leverancier: Bioss
Omschrijving: Ion channel gated by extracellular ATP involved in a variety of cellular responses, such as excitatory postsynaptic responses in sensory neurons, neuromuscular junctions (NMJ) formation, hearing, perception of taste and peristalsis. In the inner ear, regulates sound transduction and auditory neurotransmission, outer hair cell electromotility, inner ear gap junctions, and K(+) recycling. Mediates synaptic transmission between neurons and from neurons to smooth muscle.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-4065R-A750

Anti-ATP receptor Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalogus nummer: (BOSSBS-4065R-A750)
Leverancier: Bioss
Omschrijving: Ion channel gated by extracellular ATP involved in a variety of cellular responses, such as excitatory postsynaptic responses in sensory neurons, neuromuscular junctions (NMJ) formation, hearing, perception of taste and peristalsis. In the inner ear, regulates sound transduction and auditory neurotransmission, outer hair cell electromotility, inner ear gap junctions, and K(+) recycling. Mediates synaptic transmission between neurons and from neurons to smooth muscle.
UOM: 1 * 100 µl
Product Image-620-1858

VWR® Traceable®, Grootcijferige Alarmthermometer

Catalogus nummer: (620-1858)
Leverancier: VWR Collection
Omschrijving: Deze digitale thermometer maakt het gelijktijdig aflezen van omgevings- en sondetemperaturen mogelijk. Een hoorbaar alarm klinkt bij hoge/lage temperaturen, tussen twee instellingen en buiten twee instellingen. Groen/rood licht en alarm worden geactiveerd wanneer de toestand 'buiten bereik' wordt gedetecteerd.
UOM: 1 * 1 ST
Image Unavailable-HUBE3055.0002.01

Circulatiekoelthermostaten, minikoeler en unikoelers

Leverancier: HUBER
Omschrijving: Veel toepassingen zijn afhankelijk van een betrouwbare koelbron. Circulatiekoelers in de unikoelerreeks zijn een ideale oplossing voor milieuvriendelijke en economische koeling in laboratoria en de industrie. Er zijn meer dan 50 verschillende lucht- en watergekoelde modellen met een koelvermogen van 0,3 tot 50 kW. Dankzij efficiënt energiebeheer zijn de gebruikskosten laag en wordt minder vers water verbruikt. Circulatiekoelers van Huber bieden een milieuvriendelijke oplossing met snel rendement.

Image Unavailable-BOSSBS-11060R-CY5

Anti-OTOA Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-11060R-CY5)
Leverancier: Bioss
Omschrijving: Otoancorin, also known as OTOA, CT108 or DFNB22, is a 1,153 amino acid protein belonging to the stereocilin family. Expressed in the inner ear and restricted to the interface between the apical surface of sensory epithelia, otoancorin is suggested to act as an adhesion molecule. Otoancorin ensures the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in the gene encoding otoancorin leads to deafness autosomal recessive type 22 (DFNB22), which is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain or the area of the brain that receives sound information. Existing as three alternatively spliced isoforms, otoancorin is encoded by a gene located on human chromosome 16p12.2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11060R-A680

Anti-OTOA/DFNB22 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalogus nummer: (BOSSBS-11060R-A680)
Leverancier: Bioss
Omschrijving: Otoancorin, also known as OTOA, CT108 or DFNB22, is a 1153 amino acid protein belonging to the stereocilin family. Expressed in the inner ear and restricted to the interface between the apical surface of sensory epithelia, otoancorin is suggested to act as an adhesion molecule. Otoancorin ensures the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in the gene encoding otoancorin leads to deafness autosomal recessive type 22 (DFNB22), which is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain or the area of the brain that receives sound information. Existing as three alternatively spliced isoforms, otoancorin is encoded by a gene located on human chromosome 16p12.2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11264R-CY7

Anti-MYO6 Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-11264R-CY7)
Leverancier: Bioss
Omschrijving: Myosin VI a molecular motor involved in intracellular vesicle and organelle transport, is the only Myosin motor that binds to the pointed end of Actin. This unique Myosin has only one light chain in the lever-arm domain and has highly irregular stepping with a wide range of step sizes, unlike that of other characterized Myosins. It associates with Clathrin-coated vesicles and disabled 2, indicating a role for Myosin VI in endocytosis. Mouse Myosin VI is expressed within the sensory hair cells of the cochlea. Human Myosin VI is mapped to the centromeric region of chromosome 6, a region that shows syntenic homology with the corresponding mouse chromosome 9 region, where the Snell’s Waltzer mutation is located. The behavioral effects of the mouse Snell’s Waltzer mutation are lack of responsiveness to sound, hyperactivity, head tossing and circling, due to the disorganization and fusing of stereocilia bundles within the inner ear. Defects of Myosin VI cause autosomal dominant nonsyndromic sensori-neural deafness in humans. Human Myosin VI is expressed in fetal cochlea and brain, as well as in adult brain.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11264R-A647

Anti-MYO6 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalogus nummer: (BOSSBS-11264R-A647)
Leverancier: Bioss
Omschrijving: Myosin VI a molecular motor involved in intracellular vesicle and organelle transport, is the only Myosin motor that binds to the pointed end of Actin. This unique Myosin has only one light chain in the lever-arm domain and has highly irregular stepping with a wide range of step sizes, unlike that of other characterized Myosins. It associates with Clathrin-coated vesicles and disabled 2, indicating a role for Myosin VI in endocytosis. Mouse Myosin VI is expressed within the sensory hair cells of the cochlea. Human Myosin VI is mapped to the centromeric region of chromosome 6, a region that shows syntenic homology with the corresponding mouse chromosome 9 region, where the Snell’s Waltzer mutation is located. The behavioral effects of the mouse Snell’s Waltzer mutation are lack of responsiveness to sound, hyperactivity, head tossing and circling, due to the disorganization and fusing of stereocilia bundles within the inner ear. Defects of Myosin VI cause autosomal dominant nonsyndromic sensori-neural deafness in humans. Human Myosin VI is expressed in fetal cochlea and brain, as well as in adult brain.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11264R-FITC

Anti-MYO6 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalogus nummer: (BOSSBS-11264R-FITC)
Leverancier: Bioss
Omschrijving: Myosin VI a molecular motor involved in intracellular vesicle and organelle transport, is the only Myosin motor that binds to the pointed end of Actin. This unique Myosin has only one light chain in the lever-arm domain and has highly irregular stepping with a wide range of step sizes, unlike that of other characterized Myosins. It associates with Clathrin-coated vesicles and disabled 2, indicating a role for Myosin VI in endocytosis. Mouse Myosin VI is expressed within the sensory hair cells of the cochlea. Human Myosin VI is mapped to the centromeric region of chromosome 6, a region that shows syntenic homology with the corresponding mouse chromosome 9 region, where the Snell’s Waltzer mutation is located. The behavioral effects of the mouse Snell’s Waltzer mutation are lack of responsiveness to sound, hyperactivity, head tossing and circling, due to the disorganization and fusing of stereocilia bundles within the inner ear. Defects of Myosin VI cause autosomal dominant nonsyndromic sensori-neural deafness in humans. Human Myosin VI is expressed in fetal cochlea and brain, as well as in adult brain.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11264R-CY3

Anti-MYO6 Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-11264R-CY3)
Leverancier: Bioss
Omschrijving: Myosin VI a molecular motor involved in intracellular vesicle and organelle transport, is the only Myosin motor that binds to the pointed end of Actin. This unique Myosin has only one light chain in the lever-arm domain and has highly irregular stepping with a wide range of step sizes, unlike that of other characterized Myosins. It associates with Clathrin-coated vesicles and disabled 2, indicating a role for Myosin VI in endocytosis. Mouse Myosin VI is expressed within the sensory hair cells of the cochlea. Human Myosin VI is mapped to the centromeric region of chromosome 6, a region that shows syntenic homology with the corresponding mouse chromosome 9 region, where the Snell’s Waltzer mutation is located. The behavioral effects of the mouse Snell’s Waltzer mutation are lack of responsiveness to sound, hyperactivity, head tossing and circling, due to the disorganization and fusing of stereocilia bundles within the inner ear. Defects of Myosin VI cause autosomal dominant nonsyndromic sensori-neural deafness in humans. Human Myosin VI is expressed in fetal cochlea and brain, as well as in adult brain.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11264R-CY5

Anti-MYO6 Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-11264R-CY5)
Leverancier: Bioss
Omschrijving: Myosin VI a molecular motor involved in intracellular vesicle and organelle transport, is the only Myosin motor that binds to the pointed end of Actin. This unique Myosin has only one light chain in the lever-arm domain and has highly irregular stepping with a wide range of step sizes, unlike that of other characterized Myosins. It associates with Clathrin-coated vesicles and disabled 2, indicating a role for Myosin VI in endocytosis. Mouse Myosin VI is expressed within the sensory hair cells of the cochlea. Human Myosin VI is mapped to the centromeric region of chromosome 6, a region that shows syntenic homology with the corresponding mouse chromosome 9 region, where the Snell’s Waltzer mutation is located. The behavioral effects of the mouse Snell’s Waltzer mutation are lack of responsiveness to sound, hyperactivity, head tossing and circling, due to the disorganization and fusing of stereocilia bundles within the inner ear. Defects of Myosin VI cause autosomal dominant nonsyndromic sensori-neural deafness in humans. Human Myosin VI is expressed in fetal cochlea and brain, as well as in adult brain.
UOM: 1 * 100 µl
Product Image-461-0098

Optionele upgrade

Leverancier: HUBER
Omschrijving: De Pilot ONE®-regelaars kunnen worden bijgewerkt voor meer flexibiliteit na de aankoop met behulp van de eenvoudig te gebruiken Plug and Play-technologie. Upgrades met extra functionaliteit zijn heel eenvoudig, u hoeft alleen een activeringscode in te voeren. Alle bovengenoemde apparaten worden geleverd met 'Basic' Pilot ONE®-regelaars die kunnen worden bijgewerkt naar <B>Pilot ONE® </B>'Exclusive' met extra functies.

Product Image-521-4174

Biosafe benchtop ultracentrifuge System, Optima™ Max-XP

Catalogus nummer: (521-4174)
Leverancier: Beckman Coulter
Omschrijving: The Optima MAX-XP's convenient touch-screen control features easy-to-read displays for gauging real-time speed, time, and temperature. The customisable user interface allows personalisation of easy-to-identify icons for up to twelve individuals, as well as sound and volume options. Multiple language capability: Access to an array of languages increases the Optima MAX-XP's functionality, anywhere in the world. From French and Spanish to Japanese, simplified Chinese and more, the Optima MAX-XP's ability to work in multiple languages enhances its value for laboratories around the world.
UOM: 1 * 1 ST
Bel voor prijs
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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