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Leverancier: Ansell
Omschrijving: Deze nylon voering met nitril coating op de palm is uitgerust met Ansell Grip Technology™. De microscopische kanalen in de coating van de handschoen voeren de olie af, dit resulteert in een stevige grip op het oppervlak. Hierdoor kunnen de gebruikers op een veilige manier kleine en middelgrote geoliede onderdelen hanteren.

Catalogus nummer: (BOSSBS-11060R-A488)
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


Catalogus nummer: (BOSSBS-11060R-HRP)
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


Catalogus nummer: (BOSSBS-11060R-CY7)
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


Catalogus nummer: (TEST0554.0452)
Leverancier: Testo
Omschrijving: Sound level calibrator, for regular calibration of testo 815, testo 816, testo 816-1
UOM: 1 * 1 ST


Catalogus nummer: (TEST0563.8155)
Leverancier: Testo
Omschrijving: Easy to use digital sound level meter with wide dynamic range, 32 to 130 dB in the frequency range 31,5 Hz to 8 kHz.
UOM: 1 * 1 ST


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


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


Catalogus nummer: (139-0082)
Leverancier: Metro International
Omschrijving: Transportwagen, Post-mount cable/tube management clips
UOM: 1 * 1 ST


Catalogus nummer: (TEST0563.8170)
Leverancier: Testo
Omschrijving: The testo 816-1 dB meter is the professional model in the Testo range of sound measuring instruments.
UOM: 1 * 1 ST


Catalogus nummer: (BOSSBS-11264R-A555)
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


Catalogus nummer: (906-0124)
Leverancier: VWR Collection
Omschrijving: The newly developed ChromAssist Data Station combines the proven intuitive structure of the Hitachi software family with an innovative new design. As a chromatography data system (CDS), ChromAssist contains all the necessary functions for controlling VWR® Hitachi HPLC and UHPLC instruments, including method creation, sample table, data integration and reporting.
UOM: 1 * 1 ST


Catalogus nummer: (521-4268)
Leverancier: Thermo Scientific
Omschrijving: Centrifuge, tafelmodel, SECURE-Spin, advanced user management and centralised monitoring features on Thermo Scientific general purpose pro centrifuges, for 1,6 and 4 L capacities, maximum 25830×g
UOM: 1 * 1 ST


Leverancier: UPM Biomedicals
Omschrijving: <B>GrowDex®-T Hydrogel</B> is a bio-friendly hydrogel extracted from birch and sourced from sustainable and responsibly managed forests.

Catalogus nummer: (BOSSBS-11264R-A350)
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


Catalogus nummer: (BOSSBS-11264R-A488)
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


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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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