You Searched For: Polyethylene+glycol+8,000


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Supplier: 3M
Description: Standard faceseal, Versaflo™

Catalog Number: (BOSSBS-6643R-A488)
Supplier: Bioss
Description: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-6643R-FITC)
Supplier: Bioss
Description: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.
UOM: 1 * 100 µl


Supplier: Corning
Description: Discharge tube, bent, protective sleeve, 2.5 - 10 ml, Corning®

Catalog Number: (111-2180)
Supplier: 3M
Description: Replacement filter pack with O-rings
UOM: 1 * 5 items


Catalog Number: (BOSSBS-2663R-CY3)
Supplier: Bioss
Description: Functions as a positive regulator of osteoclastogenesis. Cell surface receptor that signals via TYROBP. Regulates inflammatory responses. Acts as a key regulator of synovial injury and bone erosion during autoimmune joint inflammation. Critical macrophage receptor for dengue virus serotypes 1-4. The binding of dengue virus to CLEC5A triggers signaling through phosphylation of TYROBP, this interaction does not result in viral entry but stimulates proinflammatory cytokine release.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-6325R-CY5.5)
Supplier: Bioss
Description: Defects in SLC2A10 are the cause of arterial tortuosity syndrome (ATS) [MIM:208050]. ATS is an autosomal recessive disorder characterized by tortuosity and elongation of major arteries, often resulting in death at young age. Other typical features include aneurysms of large arteries and stenosis of the pulmonary artery, in association with facial features and several connective tissue manifestations such as soft skin and joint laxity. Histopathological findings include fragmentation of elastic fibers in the tunica media of large arteries.
UOM: 1 * 100 µl


Supplier: UPCHURCH SCIENTIFIC
Description: PEEK.

Catalog Number: (SCOT290320007)
Supplier: DWK Life Sciences
Description: Polyoxymethylene, coloured.
UOM: 1 * 1 items


Catalog Number: (ANSEYE30W-00215-02)
Supplier: Ansell
Description: This apron is made from an external film barrier layer with two non woven layers underneath. The fabric provides a strong liquid and particle barrier.
UOM: 1 * 30 items


Catalog Number: (HOPE20.400)
Supplier: Medicom
Description: These disposable sleeve protectors made of PP with PE coating protect the arms against dirt.
UOM: 1 * 100 items


Supplier: SciLabware
Description: PYREX®, borosilicate glass, Quickfit® joints, clear.

Catalog Number: (NEUB0970-80-1403)
Supplier: NEUBERT VOLUME GLASSWAERE
Description: Standard cone with 8 mm right angle bent olive.
UOM: 1 * 1 items


Catalog Number: (SCOT290330008)
Supplier: DWK Life Sciences
Description: Metal.
UOM: 1 * 1 items


Catalog Number: (BOSSBS-3860R-A488)
Supplier: Bioss
Description: CHRDL2 is a novel chordin like protein that can act as a BMP antagonist. Amember of the chordin family of proteins, it contains a signal peptide andthree CR (cysteine-rich repeat) domains. When expressed as a recombinantprotein it is secreted and binds to activin A, but not to BMP-2, -4, -6. Differential expression has been detected in developing chondrocytes, myoblasts, osteoblasts, and osteoarthritic joints. Complex alternative splicing of CHRDL2 potentially results in distinct isoforms that differ at their C termini, in the expression of signal peptide, and in the content of CR domains. CHRDL2 was originally characterized as a novel protein exclusively expressed in breast, lung, and colon tumors.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-3860R-CY3)
Supplier: Bioss
Description: CHRDL2 is a novel chordin like protein that can act as a BMP antagonist. Amember of the chordin family of proteins, it contains a signal peptide andthree CR (cysteine-rich repeat) domains. When expressed as a recombinantprotein it is secreted and binds to activin A, but not to BMP-2, -4, -6. Differential expression has been detected in developing chondrocytes, myoblasts, osteoblasts, and osteoarthritic joints. Complex alternative splicing of CHRDL2 potentially results in distinct isoforms that differ at their C termini, in the expression of signal peptide, and in the content of CR domains. CHRDL2 was originally characterized as a novel protein exclusively expressed in breast, lung, and colon tumors.
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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