In my experience, DNA purified from agarose gels contains transformation poisons. I once demonstrated this by gel purifying covalent closed circular plasmid. The gel-purified DNA yielded 100-1000X fewer transformants/ug (depending on isolation technique). Youll get higher cloning efficiency if you purify your genomic digest on sucrose gradients and just analyze small aliquots to find the desired size fraction. If you can, avoid gel purification of the vector also, so much the better. Regards, John Thompson Gianluca Molla ,molla at imiucca.csi.unimi.it, wrote: ,Hello to everyone. ,Is the first time I write to this NG although I read ,the posts for more than one year. ,In our lab we are trying to construct a genomic library ,from a yeast (R. gracilis). We extract genomic DNA, ,digest it with EcoRI, run the digestion fragments on an ,agarose gel, extract the DNA from 7.5 to 9 kb from the gel (this is the ,size of fragments we are interested in) and ligate them to a cloning ,vector. The number of ...
Nucleic acids from ATCC Genuine Cultures can save you the time and expense of isolating DNA yourself. ATCC offers genomic DNA from well-characterized and authenticated fungal and yeast strains.
Nucleic acids from ATCC Genuine Cultures can save you the time and expense of isolating DNA yourself. ATCC offers genomic DNA from well-characterized and authenticated fungal and yeast strains.
The development of high-throughput and large-scale technologies have expanded the screening capacity for human-yeast complementation pairs. As a result, several systematic screens have reported testing the essential yeast genes for replaceability (Zhang et al. 2003; Hamza et al. 2015; Kachroo et al. 2015; Sun et al. 2016; Yang et al. 2017; Garge et al. 2019; Laurent et al. 2019). These studies generated overlapping lists of human-yeast complementation pairs and arrived at similar conclusions regarding features that predict the replaceability of essential yeast genes. However, compared to the essential yeast genes, the nonessential genes are a much larger set and have a variety of different phenotypic readouts, making them more difficult to screen systematically for complementation. In this study, we have started this process by focusing on a subset of the nonessential yeast genes, specifically those required for chromosome maintenance. We identified 20 complementation pairs that are replaceable ...
The Saccharomyces cerevisiae SNF2 gene affects the expression of many diversely regulated genes and has been implicated in transcriptional activation. We report here the cloning and characterization of STH1, a gene that is homologous to SNF2. STH1 is essential for mitotic growth and is functionally distinct from SNF2. A bifunctional STH1-beta-galactosidase protein is located in the nucleus. The predicted 155,914-Da STH1 protein is 72% identical to SNF2 over 661 amino acids and 46% identical over another stretch of 66 amino acids. Both STH1 and SNF2 contain a putative nucleoside triphosphate-binding site and sequences resembling the consensus helicase motifs. The large region of homology shared by STH1 and SNF2 is conserved among other eukaryotic proteins, and STH1 and SNF2 appear to define a novel family of proteins related to helicases. ...
ID YEP367 preliminary; circular DNA; SYN; 8400 BP. XX AC ATCC37735; XX DT 01-JUL-1993 (Rel. 7, Created) DT 01-JUL-1995 (Rel. 12, Last updated, Version 1) XX DE Saccharomyces/E.coli plasmid vector YEp367 - incomplete. XX KW cloning vector. XX OS Cloning vector OC Artificial sequences; Cloning vehicles. XX RN [1] RC YEp352E from YEp352 & linker RC YEp363A from pNM480 & YEp351 RC YEp353A from pNM480 & YEp352 RC YEp353 from YEp353A & YEp352E RC YEp354A from pNM481 & YEp352 RC YEp354 from YEp354A & YEp352E RC YEp355A from pNM482 & YEp352 RC YEp355 from YEp355A & YEp352E RC YEp356, YEp356R from YEp353 & pUC18 RC YEp357, YEp357R from YEp354 & pUC18 RC YEp358, YEp358R from YEp355 & pUC18 RC YEp363 from YEp363A & YEp353 RC YEp364 from YEp363A & YEp354 RC YEp365 from YEp363A & YEp355 RC YEp366 from YEp363A & YEp356 RC YEp367 from YEp363A & YEp357 RC YEp368 from YEp363A & YEp358 RC YEp366R from YEp363A & YEp356R RC YEp367R from YEp363A & YEp357R RC YEp368R from YEp363A & YEp358R RC YIp353 from YEp353 & ...
ID YEP353 preliminary; circular DNA; SYN; 7944 BP. XX AC U03500; ATCC37725; XX DT 01-JUL-1993 (Rel. 7, Created) DT 01-JUL-1995 (Rel. 12, Last updated, Version 1) XX DE Saccharomyces/E.coli plasmid vector YEp353 - complete. XX KW cloning vector. XX OS Cloning vector OC Artificial sequences; Cloning vehicles. XX RN [1] RP 1-7944 RC YEp352E from YEp352 & linker RC YEp363A from pNM480 & YEp351 RC YEp353A from pNM480 & YEp352 RC YEp353 from YEp353A & YEp352E RC YEp354A from pNM481 & YEp352 RC YEp354 from YEp354A & YEp352E RC YEp355A from pNM482 & YEp352 RC YEp355 from YEp355A & YEp352E RC YEp356, YEp356R from YEp353 & pUC18 RC YEp357, YEp357R from YEp354 & pUC18 RC YEp358, YEp358R from YEp355 & pUC18 RC YEp363 from YEp363A & YEp353 RC YEp364 from YEp363A & YEp354 RC YEp365 from YEp363A & YEp355 RC YEp366 from YEp363A & YEp356 RC YEp367 from YEp363A & YEp357 RC YEp368 from YEp363A & YEp358 RC YEp366R from YEp363A & YEp356R RC YEp367R from YEp363A & YEp357R RC YEp368R from YEp363A & YEp358R RC YIp353 ...
TY - JOUR. T1 - The Saccharomyces cerevisiae gene SDS22 encodes a potential regulator of the mitotic function of yeast type 1 protein phosphatase. AU - MACKELVIE, SARAH H. AU - ANDREWS, PAUL D.. AU - STARK, MICHAEL J. R. PY - 1995/7. Y1 - 1995/7. N2 - In higher eukaryotes, the activity and specificity of the type 1 protein serine-threonine phosphatase (PP1) catalytic subunit is thought to be controlled by its association with a number of regulatory or targeting subunits. Here we describe the characterization of a gene encoding one such potential polypeptide in the yeast Saccharomyces cerevisiae. The gene which we have isolated (termed SDS22) encodes a product with a high degree of sequence identity to the fission yeast sds22 protein, a known regulator of the mitotic function of PP1 in Schizosaccharomyces pombe. Using two different criteria, we have demonstrated that Sds22p and the catalytic subunit of PP1 (Glc7p) interact in yeast cells. We have also generated a temperature-sensitive allele of ...
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We have isolated STN1, an essential Saccharomyces cerevisiae gene, as a suppressor of the cdc13-1 mutation. A synthetic lethal interaction between a temperature-sensitive mutant allele of STN1, stn1-13, and cdc13-1 was observed. Stn1 and Cdc13 proteins displayed a physical interaction by two-hybrid analysis. As shown previously for cdc13-1, stn1-13 cells at the restrictive temperature accumulate single-stranded DNA in subtelomeric regions of the chromosomes, but to a lesser extent than cdc13-1 cells. In addition, both Cdc13 and Stn1 were found to be involved in the regulation of telomere length, mutations in STN1 or CDC13 conferring an increase in telomere size. Loss of Stn1 function activated the RAD9 and MEC3 G2/M checkpoints, therefore confirming that DNA damage is generated. We propose that Stn1 functions in telomere metabolism during late S phase in cooperation with Cdc13 ...
New Sequences ============= S82971 S82971 1775bp DNA PLN 10-FEB-1997 PEX13=PAS20 [Saccharomyces cerevisiae, Genomic, 1775 nt]. PEX13; Pex13p. SCRGA1 X90950 4305bp DNA PLN 07-FEB-1997 S.cerevisiae rga1 (dbm1) gene. DBM1; pheromone response; RGA1 gene; RGA1 (DBM1); Rga1p (Dbm1p). SCU17262 U17262 3051bp DNA PLN 11-FEB-1997 Saccharomyces cerevisiae Pip1p (PIP1) gene, complete cds. PIP1; Pip1p. SCU17263 U17263 2251bp DNA PLN 11-FEB-1997 Saccharomyces cerevisiae Pip2p (PIP2) gene, complete cds. PIP2; Pip2p. SCU17264 U17264 1842bp DNA PLN 11-FEB-1997 Saccharomyces cerevisiae Pip3p (PIP3) gene, complete cds. PIP3; Pip3p. SCU85960 U85960 1720bp DNA PLN 11-FEB-1997 Saccharomyces cerevisiae RNA polymerase II-specific TBP associated factor Taf40p (TAF40) gene, complete cds. TAF40; RNA polymerase II specific TBP associated; factor. SCU86641 U86641 1657bp DNA PLN 08-FEB-1997 Saccharomyces cerevisiae Rim9p (RIM9) gene, complete cds. RIM9; Rim9p. =========== Updated Features/Annotations ============= YSCDYS1 ...
Sequence analysis of a 33.1 kb fragment from the left arm of Saccharomyces cerevisiae chromosome X, including putative proteins with leucine zippers, a fungal Zn(11)2-Cys6 binuclear cluster domin and a putative alpha2-SCB-alpha2 binding site ...
TY - JOUR. T1 - Molecular cloning and characterization of the RAD1 gene of Saccharomyces cerevisiae. AU - Higgins, David R.. AU - Prakash, Satya. AU - Reynolds, Paul. AU - Prakash, Louise. PY - 1983. Y1 - 1983. N2 - We have cloned the RAD1 gene of Saccharomyces cerevisiae and physically mapped it to a 4.0-kb DNA fragment from chromosome XVI. The RAD1 gene determines a transcript of 3.1 kb, and the direction of transcription was found to be leftwards, from EcoRI towards BglII (Fig. 1). Deletions of the RAD1 gene were made and were found to have no effect on viability of vegetative cells or spores, or on sporulation.. AB - We have cloned the RAD1 gene of Saccharomyces cerevisiae and physically mapped it to a 4.0-kb DNA fragment from chromosome XVI. The RAD1 gene determines a transcript of 3.1 kb, and the direction of transcription was found to be leftwards, from EcoRI towards BglII (Fig. 1). Deletions of the RAD1 gene were made and were found to have no effect on viability of vegetative cells or ...
SPT16 was previously identified as a high-copy-number suppressor of delta insertion mutations in the 5 regions of the HIS4 and LYS2 genes of Saccharomyces cerevisiae. We have constructed null mutations in the SPT16 gene and have demonstrated that it is essential for growth. Temperature-sensitive-lethality spt16 alleles have been isolated and shown to be pleiotropic; at a temperature permissive for growth, spt16 mutations suppress delta insertion mutations, a deletion of the SUC2 upstream activating sequence, and mutations in trans-acting genes required for both SUC2 and Ty expression. In addition, SPT16 is identical to CDC68, a gene previously shown to be required for passage through the cell cycle control point START. However, at least some transcriptional effects caused by spt16 mutations are independent of arrest at START. These results and those in the accompanying paper (A. Rowley, R. A. Singer, and G. C. Johnston, Mol. Cell. Biol. 11:5718-5726, 1991) indicate that SPT16/CDC68 is required ...
TY - JOUR. T1 - A DNA integrity network in the yeast Saccharomyces cerevisiae. AU - Pan, Xuewen. AU - Ye, Ping. AU - Yuan, Daniel S.. AU - Wang, Xiaoling. AU - Bader, Joel S.. AU - Boeke, Jef D.. N1 - Funding Information: We thank members of the Boeke lab for valuable discussions and Pamela Meluh for critical comments on the manuscript. We thank Brian Peyser and Forrest Spencer for valuable discussions on synthetic lethality networks, Heng Zhu for the GAL1pr-GST-CTF4 and GAL1pr-GST overexpression plasmids, Alain Verreault for the GAL1pr-HHT plasmid, and Ivana Celic for sharing unpublished data. Raw data were submitted to GEO (Accession #GSE3574). We regret inability to cite many relevant studies of DNA metabolism and genomic instability due to space limits. Under a licensing agreement between Open Biosystems, Inc. and the Johns Hopkins University, the University is entitled to a share of royalties on sales of yeast strains described in this article. The terms of this arrangement are being ...
Evolution of multigene families are considered in the review on the example of the PHO gene family encoding the structure of acid phosphatases in the yeast Saccharomyces cerevisiae. Analysis of the...
TY - THES. T1 - Lipid transport to the plasma membrane of the yeast Saccharomyces cerevisiae. AU - Pichler, Harald. PY - 2000. Y1 - 2000. M3 - Doctoral Thesis. ER - ...
Saccharomyces cerevisiae Protein STE5 (STE5) ,partial datasheet and description hight quality product and Backed by our Guarantee
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TY - JOUR. T1 - Increased stress parameter synthesis in the yeast Saccharomyces cerevisiae after treatment with 4-hydroxy-2-nonenal. AU - Wonisch, Willibald. AU - Hayn, Marianne. AU - Schaur, Jörg. AU - Tatzber, Franz. AU - Kranner, Ilse. AU - Grill, Dieter. AU - Winkler, Rudolf. AU - Bilinski, Tomasz. AU - Kohlwein, Sepp-Dieter. AU - Esterbauer, Hermann. PY - 1997. Y1 - 1997. U2 - 10.1016/S0014-5793(97)00123-3. DO - 10.1016/S0014-5793(97)00123-3. M3 - Article. VL - 405. SP - 11. EP - 15. JO - FEBS letters. JF - FEBS letters. SN - 0014-5793. IS - 1. ER - ...
This unit presents detailed protocols for a range of centrifugation‐based subcellular fractionation procedures for the yeast Saccharomyces cerevisiae
Yeast Saccharomyces cerevisiae in vivo Prp8 splicing assay(A) Schematic representation of the two-step splicing pathway (SS, splice site; BS, branch site). Brie
MOTIZUKI, M., MITSUI, K., ENDO, Y. and TSURUGI, K. (1986), Detection and partial characterization of the chromatin-associated proteases of yeast Saccharomyces cerevisiae. European Journal of Biochemistry, 158: 345-350. doi: 10.1111/j.1432-1033.1986.tb09757.x ...
Budding Yeast: Saccharomyces cerevisiae Saccharomyces cerevisiae, the budding yeast, is the common yeast used in baking (bakers yeast) and brewing (brewers
TY - CHAP. T1 - Lipids and membranes in Saccharomyces cerevisiae.. AU - Schweizer, Michael. PY - 1999. Y1 - 1999. M3 - Chapter. SP - 79. EP - 155. BT - In The Metabolism & Molecular Physiology of Saccharomyces cerevisiae. Eds. J R Dickinson & M Schweizer. Taylor & Francis, London. ER - ...
Biosprint® is an active yeast (Saccharomyces cerevisiae MUCL 39885) used for animal feed. Biosprint is authorized by the European Union as feed additive for piglets, cattle for fattening, dairy cows, horses and sows.
Saccharomyces cerevisiae ATCC ® 9763D-5™ Designation: Genomic DNA from Saccharomyces cerevisiae NRRL Y-567 (ATCC ® 9763™) Application: Food testing
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1P-022 Saccharomyces cerevisiaeの糖代謝における転写制御ネットワークの予測(遺伝子工学,一般講演)1P-022 Saccharomyces cerevisiaeの糖代謝における転写制御ネットワークの予測(遺伝子工学,一般講演)AN10549378 ...
The Saccharomyces Cerevisiae Morphological Database(SCMD) is a collection of micrographs of budding yeast mutants. Micorgraphs of mutants with altered cell morphology were taken at Ohya Group, University of Tokyo, from a set of the haploid MATa deleted strains obtained from EUROSCARF. From the micrographs, disruptant cells are automatically extracted by our novel cell-image processing software developed at Morishita Group, University of Tokyo. Heterozygous essential gene deletion set, DAmP collection set, natural yeast strain set and others were analyzed by this software. ...
The Saccharomyces Genome Database (SGD) provides comprehensive integrated biological information for the budding yeast Saccharomyces cerevisiae.
TY - JOUR. T1 - Degradation of HMG-CoA reductase-induced membranes in the fission yeast, Schizosaccharomyces pombe. AU - Lum, Pek Yee. AU - Wright, Robin. PY - 1995/10/1. Y1 - 1995/10/1. N2 - Elevated levels of certain membrane proteins, including the sterol biosynthetic enzyme HMG-CoA reductase, induce proliferation of the endoplasmic reticulum. When the amounts of these proteins return to basal levels, the proliferated membranes are degraded, but the molecular details of this degradation remain unknown. We have examined the degradation of HMG-CoA reductase-induced membranes in the fission yeast, Schizosaccharomyces pombe. In this yeast, increased levels of the Saccharomyces cerevisiae HMG-CoA reductase isozyme encoded by HMG1 induced several types of membranes, including karmellae, which formed a cap of stacked membranes that partially surrounded the nucleus. When expression of HMG1 was repressed, the karmellae detached from the nucleus and formed concentric, multilayered membrane whorls that ...
ERK5 is a mitogen-activated protein (MAP) kinase regulated in human cells by diverse mitogens and stresses but also suspected of mediating the effects of a number of oncogenes. Its expression in the slt2Delta Saccharomyces cerevisiae mutant rescued several of the phenotypes caused by the lack of Slt2p (Mpk1p) cell integrity MAP kinase. ERK5 is able to provide this cell integrity MAP kinase function in yeast, as it is activated by the cell integrity signaling cascade that normally activates Slt2p and, in its active form, able to stimulate at least one key Slt2p target (Rlm1p, the major transcriptional regulator of cell wall genes). In vitro ERK5 kinase activity was abolished by Hsp90 inhibition. ERK5 activity in vivo was also lost in a strain that expresses a mutant Hsp90 chaperone. Therefore, human ERK5 expressed in yeast is an Hsp90 client, despite the widely held belief that the protein kinases of the MAP kinase class are non-Hsp90-dependent activities. Two-hybrid and protein binding studies ...
Autophagy is an intracellular process responsible for the degradation and recycling of cytoplasmic components. It selectively removes harmful cellular material and enables the cell to survive starvation by mobilizing nutrients via the bulk degradation of cytoplasmic components. While research over the last decades has led to the discovery of the key factors involved in autophagy, the pathway is not yet completely understood. The first studies of autophagy on a molecular level were conducted in the yeast Saccharomyces cerevisiae. Building up on these studies, many homologs have been found in higher eukaryotes. Yeast remains a highly relevant model organism for studying autophagy, with a wide range of established methods to elucidate the molecular details of the autophagy pathway. In this review, we provide an overview of methods to study both selective and bulk autophagy, including intermediate steps in the yeast Saccharomyces cerevisiae. We compare different assays, discuss their advantages and
Saccharomyces cerevisiae is a species of budding yeast. It is perhaps the most useful yeast owing to its use since ancient times in baking and brewing. It is believed that it was originally isolated from the skins of grapes (one can see the yeast as a component of the thin white film on the skins of some dark-colored fruits such as plums; it exists among the waxes of the cuticle). It is one of the most intensively studied eukaryotic model organisms in molecular and cell biology, much like Escherichia coli as the model prokaryote. It is the microorganism behind the most common type of fermentation. Saccharomyces cerevisiae cells are round to ovoid, 5-10 micrometres in diameter. It reproduces by a division process known as budding. It is useful in studying the cell cycle because it is easy to culture, but, as a eukaryote, it shares the complex internal cell structure of plants and animals. S. cerevisiae was the first eukaryotic genome that was completely sequenced. The yeast genome database [1] is ...
Saccharomyces Cerevisiae Yeast Cells Sem Scanning as a 8x6 Glass Mount from CMSP Photo Prints. Fast and safe delivery. Saccharomyces Cerevisiae Yeast Cells. these Microorganisms Fungi are Used to Raise Bread Dough the Yeasts Produce
Read The Genetic Control of Cell Growth and Development in Yeast Saccharomyces cerevisiae: Disturbed Sporulation in Diploids with a Decreased Activity of the Ras/cAMP Signal Transduction Pathway, Russian Journal of Genetics on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
Getting Better Intestinal Health through the Addition of Yeast (Saccharomyces Cerevisiae) Combined with Threonine in Broilers Diets
Algerghina, L.; Porro, D.; Martegani, E.; Ranzi, B.M., 1991: Ethanol and biomass production from whey lactose by an engineered Saccharomyces cerevisiae strain
Ubiquitin carrier proteins (E2s) are involved in the covalent attachment of ubiquitin to a variety of cellular target proteins in eukaryotes. Here, we report the cloning of genes from wheat and Arabidopsis thaliana that encode 16-kDa E2s and a domain analysis of E2s by in vitro mutagenesis. The genes for E216kDa, which we have designated wheat and At UBC1, encode proteins that are only 33% identical (58% similar) with a 23-kDa E2 from wheat (encoded by the gene now designated wheat UBC4), but are 63% identical (82% similar) with the E2 encoded by the Saccharomyces cerevisiae DNA repair gene, RAD6. Unlike the proteins encoded by RAD6 and wheat UBC4, the UBC1 gene products lack acidic C-terminal domains extending beyond the conserved core of the proteins and are incapable of efficient in vitro ligation of ubiquitin to histones. From enzymatic analysis of the UBC1 and UBC4 gene products mutagenized in vitro, we have identified several domains important for E2 function, including the active site ...
I use this paper in my graduate genetics course. It describes a global screen for synthetic defects involving DNA integrity, which reveals a network of 16 functional modules. The paper illustrates screens based on genetic interactions (in this case, synthetic lethality or fitness defects) and the systems biology used to evaluate the results of such a screen. It also illustrates the use of Saccharomyces cerevisiae as a model system ...
Mitochondrial matrix space Mg2+ is important for many aspects of nucleotide metabolism [37, 38]. Two inner mitochondrial membrane transporters, Mrs2p and Lpe10p, are needed for group II intron splicing [16, 39]. MRS2 and LPE10 have slight sequence similarity with the bacterial Mg2+transporter CorA. Assays with a fluorescent Mg2+ indicator dye indicate that Mrs2p is part of an electrophoretic mitochondrial Mg2+ influx pathway inhibited by cobalt(III)hexaammine [30]. Mitochondrial Mg2+ levels changed with the levels of Mrs2p and Lpe10p. Mitochondrial electrophoretic Mg2+ uptake was absent in an MRS2 deletion strain. Mrs2p and Lpe10p are essential for yeast growth on nonfermentable carbon sources [38]. However they cannot substitute for each other suggesting non-redundant functions. It is possible that Mrs2p or Lpe10p is responsible for the mitochondrial Mg2+ release described in this report. However, in the previous experiments Mg2+ was taken up by energized mitochondria in an Mrs2p-dependent ...
Yeast strains and cell culture: Schizosaccharomyces pombe strains used were a haploid strain (h− leu1-32 ura4-D18 ade6-m216), a diploid strain (h−/h+ leu1-32/leu1-32 ura4-D18/ura4-D18 ade6-m210/ade6-m216), and a mutant haploid strain pim1-d1ts (h− leu1-32 ura4-D18 pim1-d1ts; Sazer and Nurse 1994), all of which are derived from strain 972 (Leupold 1970). Cell culture conditions, media composition, and genetic analyses have been described previously (Morenoet al. 1991).. nmt1 promoter regulation: Gene expression under the control of the nmt1 promoter (Maundrell 1990) in pREP3X or pREP41X (Forsburg 1993) was repressed by the inclusion of 5 μg/ml thiamine in the Edinburgh Minimal Media (EMM; Morenoet al. 1991). To derepress expression, cells were washed three times with thiamine-free EMM and grown in fresh thiamine-free EMM.. cDNA library screen and DNA manipulations: An S. pombe cDNA library (a gift from Bruce Edgar and Chris Norbury) in the pREP3X vector (Forsburg 1993) was transformed into ...
The biological interpretation of genetic interactions is a major challenge. Recently, Kelley and Ideker proposed a method to analyze together genetic and physical networks, which explains many of the known genetic interactions as linking different pathways in the physical network. Here, we extend this method and devise novel analytic tools for interpreting genetic interactions in a physical context. Applying these tools on a large-scale Saccharomyces cerevisiae data set, our analysis reveals 140 between-pathway models that explain 3765 genetic interactions, roughly doubling those that were previously explained. Model genes tend to have short mRNA half-lives and many phosphorylation sites, suggesting that their stringent regulation is linked to pathway redundancy. We also identify pivot proteins that have many physical interactions with both pathways in our models, and show that pivots tend to be essential and highly conserved. Our analysis of models and pivots sheds light on the organization of the
Yeast from Saccharomyces cerevisiae Type II; Synonym: (Bakers yeast); find Sigma-Aldrich-YSC2 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich.
Saccharomyces cerevisiae, HA12, a, ade1 ade2. Our materials are for use in the experiments developed by the yeast genetics educational network (GENE project) created by Dr. Tom Manney at Kansas State University (KSU). These experiments are great for hands-on teaching of some of the basic concepts in...
This data-set represents a genome-scale metabolomic map about amino acid metabolism in gene deletion strains as determined in Saccharomyces cerevisiae.
The Saccharomyces Genome Database (SGD) provides comprehensive integrated biological information for the budding yeast Saccharomyces cerevisiae.
TY - CHAP. T1 - Axl1p gene product (Saccharomyces cerevisiae). AU - Schmidt, Walter K.. AU - Michaelis, Susan. PY - 2004/6/30. Y1 - 2004/6/30. UR - http://www.scopus.com/inward/record.url?scp=84944035697&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=84944035697&partnerID=8YFLogxK. U2 - 10.1016/B978-0-12-079611-3.50269-X. DO - 10.1016/B978-0-12-079611-3.50269-X. M3 - Chapter. AN - SCOPUS:84944035697. SN - 9780120796113. VL - 1. SP - 879. EP - 882. BT - Aspartic and Metallo Peptidases. PB - Elsevier Inc.. ER - ...
Domain architecture and assignment details (superfamily, family, region, evalue) for YER138C from Saccharomyces cerevisiae SGD. Plus protein sequence and external database links.
Domain architecture and assignment details (superfamily, family, region, evalue) for YGL175C from Saccharomyces cerevisiae SGD. Plus protein sequence and external database links.
Domain architectures containing the following SCOP superfamilies _gap_,100950,_gap_ in Saccharomyces cerevisiae SGD. Domain architectures illustrate each occurrence of _gap_,100950,_gap_.
A time lapse experiment of Saccharomyces cerevisiae expressing GFP-tagged MCM1. MCM1 is a transcription factor involved in cell-type-specific trans...
Saccharomyces cerevisiae is a species of yeast. It is believed to be isolated from the skin of grapes. It is one of the most intensively studied eukaryot..
Domain architecture and assignment details (superfamily, family, region, evalue) for YIL065C from Saccharomyces cerevisiae FL100. Plus protein sequence and external database links.
A time lapse experiment of Saccharomyces cerevisiae expressing GFP tagged Cdc15, a protein kinase involves in cytokinesis. These phase and GFPimages ...
A time lapse experiment of Saccharomyces cerevisiae expressing GFP tagged Cln2. Cln2 is a G1 cyclin involved in regulation of the cell cycle; activate...
A time lapse experiment of Saccharomyces cerevisiae expressing GFP tagged Bck2, a Cln-independent activator of CLN1,2 expression. These phase and gfp...
Involved in the dephosphorylation of the large subunit of RNA polymerase II. Is required in late G1 for normal G1 cyclin expression, bud initiation and expression of certain genes that are periodically expressed during late G1. Associates with the SAP proteins in a cell cycle-dependent manner.
BioAssay record AID 460553 submitted by ChEMBL: Antiaging effect in Saccharomyces cerevisiae K6001 expressing uth1 mutant assessed as extension of replicative life span after 2 days.
Functional Overlap between eIF4G Isoforms in Saccharomyces cerevisiae. . Biblioteca virtual para leer y descargar libros, documentos, trabajos y tesis universitarias en PDF. Material universiario, documentación y tareas realizadas por universitarios en nuestra biblioteca. Para descargar gratis y para leer online.
Gene target information for GLR1 - glutathione-disulfide reductase GLR1 (Saccharomyces cerevisiae S288C). Find diseases associated with this biological target and compounds tested against it in bioassay experiments.