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Supplier: Abcam
Description: Anti-Eph receptor B1/NET Rabbit Monoclonal Antibody [clone: EPR6457]

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Catalog Number: (10796-710)
Supplier: Bachem Americas
Description: 5-FAM-Amylin (human), Trifluoroacetate salt, Molecular Formula: C186H271N51O61S2, CAS Registry Number [1678414-71-5] net, Source Synthetic, , Storage Conditions: -20 +/- 5 degree Celcius


Supplier: Miele
Description: Accessories for Glassware washing machines, A 3 Quarter basket cover, metal frame and wire netting (206mm x 206mm)

Catalog Number: (75817-086)
Supplier: Cayman Chemical Company
Description: For the measurement of NET-derived neutrophil elastase.


Catalog Number: (77077-628)
Supplier: ANTIBODIES.COM LLC
Description: Rabbit polyclonal antibody to NET-5 for WB and ELISA with samples derived from Human and Mouse.


Catalog Number: (G-4185.0250BA)
Supplier: Bachem Americas
Description: The dipeptide His-Pro-amide represents the initial enzymatic degradation product of TRH in plasma. CAS Number (net): 33605-69-5.


Catalog Number: (76855-772)
Supplier: ANTIBODIES.COM LLC
Description: Rabbit polyclonal antibody to Eph receptor B1 / NET for WB with samples derived from Human and Mouse.


Catalog Number: (76110-620)
Supplier: Bioss
Description: NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


Supplier: Cytiva
Description: Accessory kit for HiScale™ 26, includes 1 net and O-ring, 1 support screen, 2 ferrules and 2 fingertight stop plugs

Supplier: Bachem Americas
Description: [6366-77-4] (net)

Catalog Number: (10796-714)
Supplier: Bachem Americas
Description: Biotinyl-Amylin (human), Trifluoroacetate salt, Molecular Formula: C175H275N53O57S3, Relative Molecular Mass: 4129.63, CAS Registry Number: [1678415-18-3] net, Source: Synthetic, Storage Conditions: -20 +/- 5 degree Celcius, 0.5mg


Catalog Number: (L-1240.0050BA)
Supplier: Bachem Americas
Description: Z-KR-pNA, CAS-number (net) 108318-37-2.


Supplier: Ace Glass
Description: This heavy-wall borosilicate glass bottle has three PTFE valves with Tefzel keys.

Small Business Enterprise Product available on GSA Advantage®

Catalog Number: (77128-280)
Supplier: Prosci
Description: Anti-TSPAN5/NET-4 Goat Polyclonal Antibody


Catalog Number: (10247-480)
Supplier: Bioss
Description: HAPLN2 is a 340 amino acid protein encoded by the human gene HAPLN2. HAPLN2 belongs to the HAPLN family and contains one immunoglobulin (Ig)-like, V-type domain and two link domains. HAPLN2 mediates a firm binding of versican V2 to hyaluronic acid. HAPLN2 is believed to play a pivotal role in the formation of the hyaluronan-associated matrix in the central nervous system (CNS), which facilitates neuronal conduction and general structural stabilization. HAPLN2 may also be involved in the formation of extracellular matrices, contributing to perineuronal nets and facilitating the understanding of a functional role of these extracellular matrices. HAPLN2 is found in several nuclei throughout the midbrain and hindbrain in a perineuronal net pattern.


Catalog Number: (76109-310)
Supplier: Bioss
Description: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.


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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
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