U heeft gezocht op: Dibutyltin+maleate+(so+called)


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Catalogus nummer: (OXOIPO5173A)
Leverancier: THERMO FISHER DIAGNOSTICS
Omschrijving: A medium for determining the count of so-called infective microorganisms in butter and other dairy products.
UOM: 1 * 10 ST


Leverancier: Merck
Omschrijving: Dibutyltin oxide for synthesis, Sigma-Aldrich®
Catalogus nummer: (ENZOADISPA240J)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: GrpE (Glucose Regulated Protein E. coli) is encoded by a monocistronic E. coli gene, which is under the control of both s32 and s70 transcription factors. The GrpE protein is a so-called co-chaperone because it is known to assist the DnaK (Hsp70) protein to effectively carry out DnaK-dependent chaperone activity (i.e. protein folding, protein transport, disaggregation of heat inactivated proteins, activation of mutant protein).
UOM: 1 * 1 mg


Catalogus nummer: (BOSSBS-7626R)
Leverancier: Bioss
Omschrijving: RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-7626R-CY7)
Leverancier: Bioss
Omschrijving: RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.
UOM: 1 * 100 µl


Catalogus nummer: (1.31200.0001)
Leverancier: Merck
Omschrijving: De HY-RiSE® kit bevat een kleurenteststrip voor de hygiënecontrole, (een handmatige evaluatie van de algemene reinheid) van oppervlakken, met name in de voedingsmiddelen- en drankenindustrie. Detecteert voedingsmiddelresten en micro-organismen, zogenaamd onzichtbaar vuil, die gevaar kunnen opleveren voor de gezondheid. Het testprincipe is gebaseerd op het aantonen van NAD/NADH.
UOM: 1 * 50 ST

MSDS


Catalogus nummer: (ACRO382690050)
Leverancier: Thermo Fisher Scientific
Omschrijving: Dibutyltin dilaurate 94%
UOM: 1 * 5 g

MSDS


Catalogus nummer: (BOSSBS-7626R-CY3)
Leverancier: Bioss
Omschrijving: RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.
UOM: 1 * 100 µl


Leverancier: Thermo Fisher Scientific
Omschrijving: Dibutyltin oxide 98%
Leverancier: Merck
Omschrijving: Hematoxylin-Monohydrat (C.I. 75290) Certistain® is a dye for the specific staining of DNA in the nuclei. It is used in cytology and histology. Nuclei are stained blue, dark violet to black. Hematoxylins are mixed with trivalent positively charged metal salts and build up the so-called hematoxylin lakes, used for the selective staining of nuclei (DNA). Certistain® is the quality group for seleceted high quality dyes that fulfill all quality requirements for IVD and CE registration.
Leverancier: Thermo Fisher Scientific
Omschrijving: Dibutyltin diacetate ≥95%
Catalogus nummer: (TCIAD2466-5G)
Leverancier: TCI
Omschrijving: Dibutyltin bis(trifluoromethanesulphonate) ≥98.0% (W)
UOM: 1 * 5 g


Catalogus nummer: (BOSSBS-7626R-A555)
Leverancier: Bioss
Omschrijving: RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-7626R-HRP)
Leverancier: Bioss
Omschrijving: RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-4857R-A750)
Leverancier: Bioss
Omschrijving: HCV is a positive, single-stranded RNA virus in the Flaviviridae family. The genome is approximately 10,000 nucleotides and encodes a single polyprotein of about 3,000 amino acids. The polyprotein is processed by host cell and viral proteases into three major structural proteins and several non-structural protein necessary for viral replication. NS4B induces a specific membrane alteration that serves as a scaffold for the virus replication complex. This membrane alteration gives rise to the so-called ER-derived membranous web that contains the replication complex.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-7626R-A647)
Leverancier: Bioss
Omschrijving: RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.
UOM: 1 * 100 µl


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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