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cell+culture+flasks
Numéro de catalogue:
(BOSSBS-1135R-CY7)
Fournisseur:
Bioss
Description:
c-Src tyrosine kinase plays a critical role in signal transduction downstream of growth factor receptors, integrins and G protein-coupled receptors. We used stable isotope labeling with amino acids in cell culture (SILAC) approach to identify additional substrates of c-Src tyrosine kinase in human embryonic kidney 293T cells. We have identified 10 known substrates and interactors of c-Src and Src family kinases along with 26 novel substrates. We have experimentally validated 4 of the novel proteins (NICE-4, RNA binding motif 10, FUSE-binding protein 1 and TRK-fused gene) as direct substrates of c-Src using in vitro kinase assays and cotransfection experiments. Significantly, using a c-Src specific inhibitor, we were also able to implicate 3 novel substrates (RNA binding motif 10, EWS1 and Bcl-2 associated transcription factor) in PDGF signaling. Finally, to identify the exact tyrosine residues that are phosphorylated by c-Src on the novel c-Src substrates, we designed custom peptide microarrays containing all possible tyrosine-containing peptides (312 unique peptides) and their mutant counterparts containing a Tyr -->Phe substitution from 14 of the identified substrates. Using this platform, we identified 34 peptides that are phosphorylated by c-Src. We have demonstrated that SILAC-based quantitative proteomics approach is suitable for identification of substrates of nonreceptor tyrosine kinases and can be coupled with peptide microarrays for high-throughput identification of substrate phosphopeptides.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1135R-FITC)
Fournisseur:
Bioss
Description:
c-Src tyrosine kinase plays a critical role in signal transduction downstream of growth factor receptors, integrins and G protein-coupled receptors. We used stable isotope labeling with amino acids in cell culture (SILAC) approach to identify additional substrates of c-Src tyrosine kinase in human embryonic kidney 293T cells. We have identified 10 known substrates and interactors of c-Src and Src family kinases along with 26 novel substrates. We have experimentally validated 4 of the novel proteins (NICE-4, RNA binding motif 10, FUSE-binding protein 1 and TRK-fused gene) as direct substrates of c-Src using in vitro kinase assays and cotransfection experiments. Significantly, using a c-Src specific inhibitor, we were also able to implicate 3 novel substrates (RNA binding motif 10, EWS1 and Bcl-2 associated transcription factor) in PDGF signaling. Finally, to identify the exact tyrosine residues that are phosphorylated by c-Src on the novel c-Src substrates, we designed custom peptide microarrays containing all possible tyrosine-containing peptides (312 unique peptides) and their mutant counterparts containing a Tyr -->Phe substitution from 14 of the identified substrates. Using this platform, we identified 34 peptides that are phosphorylated by c-Src. We have demonstrated that SILAC-based quantitative proteomics approach is suitable for identification of substrates of nonreceptor tyrosine kinases and can be coupled with peptide microarrays for high-throughput identification of substrate phosphopeptides.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1135R-CY3)
Fournisseur:
Bioss
Description:
c-Src tyrosine kinase plays a critical role in signal transduction downstream of growth factor receptors, integrins and G protein-coupled receptors. We used stable isotope labeling with amino acids in cell culture (SILAC) approach to identify additional substrates of c-Src tyrosine kinase in human embryonic kidney 293T cells. We have identified 10 known substrates and interactors of c-Src and Src family kinases along with 26 novel substrates. We have experimentally validated 4 of the novel proteins (NICE-4, RNA binding motif 10, FUSE-binding protein 1 and TRK-fused gene) as direct substrates of c-Src using in vitro kinase assays and cotransfection experiments. Significantly, using a c-Src specific inhibitor, we were also able to implicate 3 novel substrates (RNA binding motif 10, EWS1 and Bcl-2 associated transcription factor) in PDGF signaling. Finally, to identify the exact tyrosine residues that are phosphorylated by c-Src on the novel c-Src substrates, we designed custom peptide microarrays containing all possible tyrosine-containing peptides (312 unique peptides) and their mutant counterparts containing a Tyr -->Phe substitution from 14 of the identified substrates. Using this platform, we identified 34 peptides that are phosphorylated by c-Src. We have demonstrated that SILAC-based quantitative proteomics approach is suitable for identification of substrates of nonreceptor tyrosine kinases and can be coupled with peptide microarrays for high-throughput identification of substrate phosphopeptides.
UOM:
1 * 100 µl
Numéro de catalogue:
(STMC09720)
Fournisseur:
STEMCELL Technologies
Description:
For culture, expansion, and drug screening of chronic and acute myeloid leukemia cells.
UOM:
1 * 1 Kit
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Numéro de catalogue:
(BOSSBS-11498R-A680)
Fournisseur:
Bioss
Description:
Olfactory sensory neurons contain olfactory receptors, which are G protein-coupled receptor proteins that localize to the cilia and display affinity for and bind to a variety of odor molecules. Olfactory neurons send their axons from the olfactory epithelium to the olfactory bulb, which is covered by the CNS basal lamina. FEZF1 (Fez family zinc finger protein 1), also known as Forebrain Embryonic Zinc Finger and Zinc finger protein 312B, is a 475 amino acid nuclear protein that is expressed in the olfactory epithelium and hypothalamus of mice. In FEZF1-deficient mice, axons of olfactory neurons do not reach the olfactory bulb, suggesting that FEXF1 is required for the penetration of olfactory axons though the basal lamina before innervation of the olfactory bulb. When FEZF1 translocates to the nucleus, it induces KRAS overexpression, resulting in activation of ERK-Signalling. Overexpression of FEZF1 leads to accelerated proliferation in cultured cells and increased tumour mass in mice. There are three isoforms of FEZF1 that are produced as a result of alternative splicing events.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-11498R-A750)
Fournisseur:
Bioss
Description:
Olfactory sensory neurons contain olfactory receptors, which are G protein-coupled receptor proteins that localize to the cilia and display affinity for and bind to a variety of odor molecules. Olfactory neurons send their axons from the olfactory epithelium to the olfactory bulb, which is covered by the CNS basal lamina. FEZF1 (Fez family zinc finger protein 1), also known as Forebrain Embryonic Zinc Finger and Zinc finger protein 312B, is a 475 amino acid nuclear protein that is expressed in the olfactory epithelium and hypothalamus of mice. In FEZF1-deficient mice, axons of olfactory neurons do not reach the olfactory bulb, suggesting that FEXF1 is required for the penetration of olfactory axons though the basal lamina before innervation of the olfactory bulb. When FEZF1 translocates to the nucleus, it induces KRAS overexpression, resulting in activation of ERK-Signalling. Overexpression of FEZF1 leads to accelerated proliferation in cultured cells and increased tumour mass in mice. There are three isoforms of FEZF1 that are produced as a result of alternative splicing events.
UOM:
1 * 100 µl
Fournisseur:
OMEGA BIO-TEK
Description:
Le kit E.Z.N.A.® Viral RNA est conçu pour l'isolement de l'ARN viral à partir de liquides exempts de cellules, tels que le plasma, le sérum, l'urine et le surnageant de culture cellulaire. Cette procédure élimine totalement les contaminants et les inhibiteurs d'enzymes, ce qui le rend l'isolement d'ARN viral rapide, pratique et fiable. Le kit est également adapté à l'isolement de l'ARN total à partir de cellules en culture, de tissus et de bactéries. L'ARN purifié à l'aide de la méthode E.Z.N.A.® Viral RNA est prêt à l'emploi pour toutes les applications en aval telles que la RT-PCR.
Numéro de catalogue:
(BOSSBS-1135R-CY5)
Fournisseur:
Bioss
Description:
c-Src tyrosine kinase plays a critical role in signal transduction downstream of growth factor receptors, integrins and G protein-coupled receptors. We used stable isotope labeling with amino acids in cell culture (SILAC) approach to identify additional substrates of c-Src tyrosine kinase in human embryonic kidney 293T cells. We have identified 10 known substrates and interactors of c-Src and Src family kinases along with 26 novel substrates. We have experimentally validated 4 of the novel proteins (NICE-4, RNA binding motif 10, FUSE-binding protein 1 and TRK-fused gene) as direct substrates of c-Src using in vitro kinase assays and cotransfection experiments. Significantly, using a c-Src specific inhibitor, we were also able to implicate 3 novel substrates (RNA binding motif 10, EWS1 and Bcl-2 associated transcription factor) in PDGF signaling. Finally, to identify the exact tyrosine residues that are phosphorylated by c-Src on the novel c-Src substrates, we designed custom peptide microarrays containing all possible tyrosine-containing peptides (312 unique peptides) and their mutant counterparts containing a Tyr -->Phe substitution from 14 of the identified substrates. Using this platform, we identified 34 peptides that are phosphorylated by c-Src. We have demonstrated that SILAC-based quantitative proteomics approach is suitable for identification of substrates of nonreceptor tyrosine kinases and can be coupled with peptide microarrays for high-throughput identification of substrate phosphopeptides.
UOM:
1 * 100 µl
Fournisseur:
Sartorius
Description:
Les dispositifs Vivaflow® 50 et 200 sont des cassettes à flux tangentiel prêtes à l'emploi pour la filtration et la concentration d'échantillons de 100 ml à 3 l, ou de 500 ml à 5 l. La surface de la membrane est de 50 cm² ou 200 cm², respectivement. Les dispositifs sont livrés avec tous les accessoires nécessaires pour un fonctionnement avec une pompe de laboratoire et une tête de pompe de taille 16. Pour accélérer la concentration et augmenter le rendement, jusqu'à six cassettes Vivaflow® 50 peuvent être reliées entre elles, ou deux unités Vivaflow® 200. Convenant aux applications telles que la concentration du surnageant de culture cellulaire, la concentration virale et la concentration aqueuse, ce produit allie facilité d'utilisation, fiabilité et flexibilité.
Fournisseur:
DWK Life Sciences
Description:
En verre borosilicaté 3.3 transparent DURAN® avec col ISO (GL 45).
Fournisseur:
Thermo Fisher Scientific
Description:
Membrane en acétate de cellulose exempt de surfactant (SFCA), boîtier en PS. Idéales pour la culture cellulaire. Faible adsorption protéique.
Fournisseur:
STEMBIOSYS
Description:
CELLvo™ Ostoeoarthritic Human Chondrocytes (50-70y) are primary, uncultured cells isolated from recently-diseased cadaver cartilage from donors between 50 and 70 years old. Osteoarthritis status is determined by macroscopic inspection using a modified Outerbridge (1960) scale. Cells are isolated by enzymatic digestion prior to cryopreservation.
Numéro de catalogue:
(444-7084)
Fournisseur:
VWR Collection
Description:
Conçu pour un grand nombre d'applications d'agitation, par ex. cultures cellulaires, études de solubilité, suspensions bactériennes ou applications de mélange classiques. La plate-forme grande capacité pour accueillir jusqu'à 15,9 kg. Commande de vitesse variable par microprocesseur permettant une agitation uniforme. Pour plus de sécurité, les agitateurs accroissent progressivement leur vitesse jusqu'à la valeur programmée. Le système d'agitation Accu-drive permet un contrôle de la vitesse, une précision, une sécurité et une durabilité exceptionnels : il assure un contrôle continu de la vitesse d'agitation et maintient la valeur programmée même en cas de changement de charge. Précision de la vitesse affichée à 1% de la vitesse définie (lorsque la vitesse est au-dessus de 100 min⁻¹).
UOM:
1 * 1 ST
Numéro de catalogue:
(BOSSBS-1967R-A680)
Fournisseur:
Bioss
Description:
Kallikrein 9, also known as Kallikrein-Like 3 (KLK-L3), is a chymotrypsin-like serine proteinase. Kallikrein 9 was discovered as the locus for kallikreins on chromosome 19 was more fully mapped and found by similarity to the other tissue kallikreins. Kallikrein 9 has been found in the ovary, thymus, testis, prostate, skin, breast and neuronal tissues and is made by many cell lines in culture. Kallikrein 9 levels in breast cancer and uterine cancer patients have been reported to drop as the disease progresses, thus hK9 might be considered a favorable prognostic marker. Different splice variants of hK9 have been reported, although it is not yet known if they produce functional proteins. The full length Kallikrein 9 encodes for a 250 amino acid protein, with a predicted mass of 27.5 kDa and a pI of 7.53. The 234 amino acid form predicts a protein of 26 kDa with a pI of 9.76 and this quite basic pI might give the shorter form a very different function or localisation. The shorter sequence also diverges before the catalytic serine residue, making it unlikely to be proteolytically active. Pre-pro-kallikrein 9 has the 17 amino acid signal sequence is removed before secretion, and the Pro-kallikrein 9 is activated to Kallikrein 9 by removal of the 5 amino acid propeptide domain.
UOM:
1 * 100 µl
Fournisseur:
Thermo Fisher Scientific
Description:
Thermo Scientific™ cell culture media for SILAC is optimised for use with stable isotope labeling with amino acids in cell culture (SILAC) to analyse protein expression by mass spectrometry (MS).
Numéro de catalogue:
(SARS83.1836.300)
Fournisseur:
SARSTEDT
Description:
PS, gamma sterilised, with lid.
UOM:
1 * 50 ST
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