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Catalog Number: (PRTWPA54BKR)
Supplier: Portwest
Description: Strong and durable precision engineered aluminium shell torch, uses new CREE technology which is up to 10 times brighter than current L.E.D bulbs.
UOM: 1 * 1 items


Catalog Number: (OPTKIM3GLASS)
Supplier: OPTIKA
Description: Inverted microscopes are useful for observing living cells or organisms at the bottom of a large container (e.g., a tissue culture flask) under more natural conditions than on a glass slide, as it occurs with a conventional microscope. IM-3 series is engineered and designed to be your ideal solution for fast and reliable routine inspections, with the exclusive, state-of-the-art X-LED8 illumination system.
UOM: 1 * 1 items


Supplier: OLYMPUS OPTICAL
Description: Accessory for microscopes, For: CKX53, Dust Cover for CKX Microscopes

Supplier: VISION ENGINEERING
Description: High productivity eyepiece-less stereo microscope.

Supplier: SAMCO
Description: These graduated pipettes feature a built-in pipette bulb that eliminates need for plugging, packaging, autoclaving while preventing cross-contamination.

Environmentally Preferable

Supplier: MOTIC
Description: Accessory for microscopes, For: Stereo zoom microscopes, Universal stand (rectangular), 400 mm

Supplier: VWR Collection
Description: Polyester, sterile, with lid. These insert plates feature a thin, microscopically transparent polyester membrane that is tissue culture-treated for optimal cell attachment and growth.

Environmentally Preferable

Supplier: MOTIC
Description: Accessory for microscopes, For: K, Eyepiece 32×/12

Supplier: MOTIC
Description: Accessory for microscopes, Five head observation optical bridge

Supplier: MOTIC
Description: Accessory for microscopes, For: B1, B3 series, Phase contrast attachment 10×

Catalog Number: (BOSSBS-11330R-A350)
Supplier: Bioss
Description: There are three sorCS genes that have diverse, partially overlapping functions in the central nervous system. In the developing and mature central nervous system, the homologous SorCS1 and SorCS2 genes and the SorCS3 gene are expressed in a combinatorial, non-overlapping pattern. SorCS proteins show homology to the mosaic receptor SorLA and the neurotensin receptor sortilin, based on a common VPS10 domain, which is the hallmark of the SorCS receptor family. SorCS1 is a type 1 receptor containing a VPS10P domain and a leucine-rich domain. Alternative splicing of human SorCS1 results in four isoforms with different cytoplasmic tails and differential expression in tissues. Human SorCS1 is detected in fetal and infant brain and in fetal retina. Alternative splicing of murine SorCS1 also results in four isoforms. Murine isoform 1 is highly expressed in brain and at lower levels in heart, liver and kidney. It is detected in newborn mouse brain and in adult olfactory bulb and cerebral cortex. Murine isoform 2 is highly expressed in liver and at lower levels in heart, brain, kidney and testis.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-11330R-CY7)
Supplier: Bioss
Description: There are three sorCS genes that have diverse, partially overlapping functions in the central nervous system. In the developing and mature central nervous system, the homologous SorCS1 and SorCS2 genes and the SorCS3 gene are expressed in a combinatorial, non-overlapping pattern. SorCS proteins show homology to the mosaic receptor SorLA and the neurotensin receptor sortilin, based on a common VPS10 domain, which is the hallmark of the SorCS receptor family. SorCS1 is a type 1 receptor containing a VPS10P domain and a leucine-rich domain. Alternative splicing of human SorCS1 results in four isoforms with different cytoplasmic tails and differential expression in tissues. Human SorCS1 is detected in fetal and infant brain and in fetal retina. Alternative splicing of murine SorCS1 also results in four isoforms. Murine isoform 1 is highly expressed in brain and at lower levels in heart, liver and kidney. It is detected in newborn mouse brain and in adult olfactory bulb and cerebral cortex. Murine isoform 2 is highly expressed in liver and at lower levels in heart, brain, kidney and testis.
UOM: 1 * 100 µl


Supplier: ZEISS
Description: Accessory for microscopes, Axio Vert, For: A1 FL-LED, Microscope stand

Supplier: HIRSCHMANN
Description: Burette, Aspirator bulb

Catalog Number: (BOSSBS-13597R-A680)
Supplier: Bioss
Description: The homeobox protein, HESX1, which is also known as Rathke?s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13597R-FITC)
Supplier: Bioss
Description: The homeobox protein, HESX1, which is also known as Rathke’s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.
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 on +353 1 88 22222.
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 on +353 1 88 22222.
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 eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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