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Masterflex+Single-use
Fournisseur:
Thermo Fisher Scientific
Description:
These columns can resolve protein isoforms that differ by a single charged residue. A thin, hydrophilic layer prevents unwanted secondary interactions. The grafted anion exchange surface provides pH based selectivity control and fast mass transfer for high efficiency separation and moderate capacity.
Fournisseur:
Thermo Fisher Scientific
Description:
Capitol Vial™ are specimen containers manufactured airtight, leak resistant and aseptic by process.
Numéro de catalogue:
(HEWL8500-6947)
Fournisseur:
Agilent
Description:
Standard de cobalt, 10 mg/L, Cobalt, Matrice: 2% HNO₃, Applications: Étalons ICP
UOM:
1 * 1 ST
Fournisseur:
EPPENDORF
Description:
Eppendorf® Conical Tubes with SnapTec® caps offer secure sample containment for diverse applications. The innovative SnapTec® Cap ensures easy, secure sealing, making them ideal for molecular biology, genomics, and more. The conical design aids optimal sample recovery, enhancing efficiency and reliability in the lab.
Numéro de catalogue:
(PRSI91-934)
Fournisseur:
ProSci Inc.
Description:
Protocadherin-10 (PCDH10) is a single-pass type I membrane protein that contains six extracellular cadherin domains, one transmembrane domain and one cytoplasmic tail differing from those of the classical cadherins. As a potential calcium-dependent cell-adhesion neuronal receptor, it may plays a role in the establishment and function of specific cell-cell connections in the brain. PCDH10 moderately expressed in all regions of the brain examined, as well as in testis and ovary, and low expression in all other tested tissues.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI91-651)
Fournisseur:
ProSci Inc.
Description:
Mannoside Acetylglucosaminyltransferase 2 (MGAT2) is a single-pass type II membrane protein that contains the typical glycosyltransferase domains: a short N-terminal cytoplasmic domain, a hydrophobic non-cleavable signal-anchor domain and a C-terminal catalytic domain. MGAT2 catalyzes an essential step in the conversion of oligo-mannose to complex N-glycans. Defects in MGAT2 are the cause of congenital disorder of glycosylation type 2A.
UOM:
1 * 50 µG
Fournisseur:
HAMILTON BONADUZ
Description:
Ces électrodes sont adaptées aux équipements KNICK® Portamess®. La tête de l'électrode crée un joint hermétique avec le tube de sockage Portamess®.
Numéro de catalogue:
(PRSI26-003)
Fournisseur:
ProSci Inc.
Description:
LRRC24 contains 1 Ig-like C2-type (immunoglobulin-like) domain and 7 LRR (leucine-rich) repeats. It is a single-pass membrane protein. The function of the LRRC24 protein remains unknown.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI55-722)
Fournisseur:
ProSci Inc.
Description:
This gene encodes a protein that is a member of the M49 family of metallopeptidases. This cytoplasmic protein binds a single zinc ion with its zinc-binding motif (HELLGH) and has post-proline dipeptidyl aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. Increased activity of this protein is associated with endometrial and ovarian cancers. Alternate transcriptional splice variants have been characterized.
UOM:
1 * 400 µl
New Product
Fournisseur:
Portwest
Description:
Anti-static, laced lab shoe manufactured from high quality, water resistant microfibre plus a single-density lightweight PU sole, resistant to oil.
Numéro de catalogue:
(PRSI26-521)
Fournisseur:
ProSci Inc.
Description:
The exact function of PURG is not known, however, it is highly similar to purine-rich element binding protein A. The latter is a DNA-binding protein which binds preferentially to the single strand of the purine-rich element termed PUR, and has been implicated in the control of both DNA replication and transcription. The exact function of this gene is not known, however, its encoded product is highly similar to purine-rich element binding protein A. The latter is a DNA-binding protein which binds preferentially to the single strand of the purine-rich element termed PUR, and has been implicated in the control of both DNA replication and transcription. This gene lies in close proximity to the Werner syndrome gene, but on the opposite strand, on chromosome 8p11. Two transcript variants encoding different isoforms have been found for this gene.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI92-591)
Fournisseur:
ProSci Inc.
Description:
Cadherin-3 (CDH3) is a single-pass type I membrane protein that belongs to the cadherin superfamily. CDH3 is a calcium-dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region, and a highly conserved cytoplasmic tail. CDH3 is expressed in some normal epithelial tissues and in some carcinoma cell lines. CDH3 preferentially interacts with themselves in a homophilic manner in connecting cells. CDH3 is involved in loss of heterosygosity events in breast and prostate cancer. Mutations in CDH3 have been associated with congential hypotrichosis with juvenile macular dystrophy.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI91-464)
Fournisseur:
ProSci Inc.
Description:
beta -1,4-galactosyltransferase 4 (B4GALT4) is a single-pass type II membrane protein that belongs to the Glycosyltransferase 7 family. B4GALT4 consist of the following 2 domains: N-Acetyllactosamine Synthase and beta -N-Acetylglucosaminyl-Glycolipid beta -1,4-Galactosyltransferase. B4GALT4 is highly expressed in the heart, placenta, kidney, and pancreas; it is lowly expressed in the brain, colon, lung, muscle, ovary, testis, and uterus. B4GALT4 function is responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids.
UOM:
1 * 50 µG
Fournisseur:
SGI - DNA Synthetic Genomics
Description:
Gibson Assembly® HiFi HC 1-Step Kits and Master Mixes allow restriction digest-free, cloning of one or more DNA fragments into virtually any location of any plasmid vector in a single round of cloning.
Numéro de catalogue:
(PRSI79-233)
Fournisseur:
ProSci Inc.
Description:
KRT18 encodes the type I intermediate filament chain keratin 18. Keratin 18, together with its filament partner keratin 8, are perhaps the most commonly found members of the intermediate filament gene family. They are expressed in single layer epithelial tissues of the body. utations in this gene have been linked to cryptogenic cirrhosis. Two transcript variants encoding the same protein have been found for this gene.
UOM:
1 * 1 EA
Numéro de catalogue:
(PRSI6783)
Fournisseur:
ProSci Inc.
Description:
TMEM106B Antibody: Transmembrane protein 106B (TMEM106B) is a single-pass transmembrane protein that is thought to be a novel risk factor for frontotemporal lobar degeneration (FTLD), a group of clinically, pathologically and genetically heterogeneous disorders associated with atrophy in the frontal lobe and temporal lobe of the brain. The actual role of TMEM106B, and that of the closely related protein TMEM106A are still undetermined.
UOM:
1 * 1 EA
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