Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Preparing word cloud

×

Search

Type in a keyword to search

Filter by last modified time
See new records

Current Facets and Filters

  • Instrument:LTQ (facet)
  • Sample Title : Descending

Facets

Sort alphabetically | Sort by count

Recent searches

PeptideAtlas provides a multi-organism, publicly accessible compendium of peptides identified in a large set of tandem mass spectrometry proteomics experiments collected for human, mouse, yeast, and several other organisms.

(last updated: Nov 28, 2017)

Data or Model Molecule

319 Results - per page

AccessionSample TitleSummaryOrganismCharacteristicsInstrumentTreatmentGrowthDigestionExtractSeparationReference
PAe000429young adults (Ati: vhl-1 deletion)young adults (Ati: vhl-1 deletion) description: young adults of a vhl-1 mutant, dissolved in 1 % Rapigest experiment type: cleavable ICAT; heavy (N2) and light (vhl-1) tag; rapigest LC-gradient: SAB_GRAD_MOD description: ? gradient programme: buffer A (10 mM KH2PO4, 25 % ACN, pH 3.0); buffer B (buffer A plus 350 mM KCl); flow 0.8 ml/min; 90 min column: 200 x 4.6 mm instrument: LTQ LC-analysis, operator: Sabine MS-analysis, operator: Sabine sample preparation: Ati, Sabine protocol: glass beads sample name: vhl-1 strain: C.elegans, vhl-1, N2 age: young adults organism, part: whole worm amount of sample: 2 mg each sample prepared on: homogenization 08.06.06 remarks: filtered before SCXLTQPMID:19260763
19260763
PAe000088Yeast, TSAA time 90 experiment, cleavable ICATTSAA time 90 experiment cleavable ICAT T=90 timepoint measures proteome expression in synchronous cells 90 min after release from alpha-factor. 2 mg TCA-precipitated protein from budding yeast cells synchronized using the mating pheromone alpha-factor were heavy-cICAT labeled, and 2 mg aynchronous baseline sample were light-cICAT labeled, 3 hrs, 37�C. Pre-labeling reduction in 5 mM TCEP, 60 min 37�C. Trypsinization in 15 ml (20 mM Tris pH 8.3, 5 mM EDTA, 12 ng/�l trypsin) 37�C overnight. Strong cation exchange on Polysulfoethyl A (PolyLC 200 mm x 4.6 mm), dogleg 800 method, 0.8 ml/min, 1 min fractions. 30 peak fractions manually avidin-purified, acid cleaved as per ABI protocol.LTQPMID:17133367
PAe000086Yeast, TSAA time 30, cleavable ICATTSAA time 30 experiment cleavable ICAT T=30 timepoint measures proteome expression in synchronous cells 30 min after release from alpha-factor. 2 mg TCA-precipitated protein from budding yeast cells synchronized using the mating pheromone alpha-factor were heavy-cICAT labeled, and 2 mg aynchronous baseline sample were light-cICAT labeled, 3 hrs, 37�C. Pre-labeling reduction in 5 mM TCEP, 60 min 37�C. Trypsinization in 15 ml (20 mM Tris pH 8.3, 5 mM EDTA, 12 ng/�l trypsin) 37�C overnight. Strong cation exchange on Polysulfoethyl A (PolyLC 200 mm x 4.6 mm), dogleg 800 method, 0.8 ml/min, 1 min fractions. 30 peak fractions manually avidin-purified, acid cleaved as per ABI protocol.LTQPMID:17133367
PAe000089Yeast, TSAA time 120 experiment, cleavable ICATTSAA time 120 experiment cleavable ICAT T=120 timepoint measures proteome expression in synchronous cells 120 min after release from alpha-factor. 2 mg TCA-precipitated protein from budding yeast cells synchronized using the mating pheromone alpha-factor were heavy-cICAT labeled, and 2 mg aynchronous baseline sample were light-cICAT labeled, 3 hrs, 37�C. Pre-labeling reduction in 5 mM TCEP, 60 min 37�C. Trypsinization in 15 ml (20 mM Tris pH 8.3, 5 mM EDTA, 12 ng/�l trypsin) 37�C overnight. Strong cation exchange on Polysulfoethyl A (PolyLC 200 mm x 4.6 mm), dogleg 800 method, 0.8 ml/min, 1 min fractions. 30 peak fractions manually avidin-purified, acid cleaved as per ABI protocol.LTQPMID:17133367
PAe000124Yeast, TSAA Time 0 ExperimentYeast test experiment. Time 0 step using original ICAT reagents. See new CL-ICAT experiments for better data.LTQ
PAe000324yeast_quality_controlyeast_quality_control Yeast cell lysate was run on LTQ, LTQ_FT and QTOF.YeastBY4741 (MATa, leu2D0, met15D0, ura3D0, his3D1)LTQYeast grown in synthetic complete medium at 30°C to log phase, harvested and diluted into 30mL synthetic complete media to a cell count of 3 × 10⁶/mL.A 150µL portion of reduced yeast protein lysate was alkylated in 25mM of iodoacetamide and diluted to 1M urea with 50mM ammonium bicarbonate. 12µg of Trypsin Gold (Promega, Madison, WI) was added to the reduced and alkylated yeast protein lysate and trypsin digest was carried out overnight at 37°C. Trypsin was inactivated by addition of glacial acetic acid and insoluble material was removed by centrifugation. Peptides were purified using 3 mL SPEC C18 columns and concentrated in a SpeedVac.After 4 h of growth at 30°C cells were harvested and washed three times with ice cold dH₂O. Cells were lysed by incubation with 1mL of ice cold 10% TCA for 1 h at 4°C. Protein precipitates were collected by centrifugation, washed twice with 1 mL cold 90% acetone, and dried in a SpeedVac (Thermo Savant, Holbrook, NY). Proteins were solubilized in 300µL of 8 M urea, 50mM ammonium bicarbonate and reduced by incubation at 56°C for 1 h in the presence of 15 mM DTT.Unfractionated.PMID:16823959
PAe000328yeast_lisa3_camyeast_lisa3_cam yeast cell lysateLTQ
PAe000326yeast_lisa2_camyeast_lisa2_cam yeast cell lysateLTQ
PAe000327yeast_lisa1_camyeast_lisa1_cam yeast cell lysateLTQ
PAe001697WCL_Hs_Tcell_WholeCellLysate9WCL_Hs_Tcell_WholeCellLysate9LTQPMID:17519225
PAe001757WCL_Hs_Tcell_WholeCellLysate8WCL_Hs_Tcell_WholeCellLysate8LTQPMID:17519225
PAe001749WCL_Hs_Tcell_WholeCellLysate7WCL_Hs_Tcell_WholeCellLysate7LTQPMID:17519225
PAe001725WCL_Hs_Tcell_WholeCellLysate6WCL_Hs_Tcell_WholeCellLysate6LTQPMID:17519225
PAe001701WCL_Hs_Tcell_WholeCellLysate5WCL_Hs_Tcell_WholeCellLysate5LTQPMID:17519225
PAe001730WCL_Hs_Tcell_WholeCellLysate4WCL_Hs_Tcell_WholeCellLysate4LTQPMID:17519225
PAe001732WCL_Hs_Tcell_WholeCellLysate3WCL_Hs_Tcell_WholeCellLysate3LTQPMID:17519225
PAe001740WCL_Hs_Tcell_WholeCellLysate2WCL_Hs_Tcell_WholeCellLysate2LTQPMID:17519225
PAe001704WCL_Hs_Tcell_WholeCellLysate14WCL_Hs_Tcell_WholeCellLysate14LTQPMID:17519225
PAe001707WCL_Hs_Tcell_WholeCellLysate13WCL_Hs_Tcell_WholeCellLysate13LTQPMID:17519225
PAe001754WCL_Hs_Tcell_WholeCellLysate12WCL_Hs_Tcell_WholeCellLysate12LTQPMID:17519225
X
  1. SciCrunch.org Resources

    Welcome to the FDI Lab - SciCrunch.org Resources search. From here you can search through a compilation of resources used by FDI Lab - SciCrunch.org and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that FDI Lab - SciCrunch.org has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on FDI Lab - SciCrunch.org then you can log in from here to get additional features in FDI Lab - SciCrunch.org such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into FDI Lab - SciCrunch.org you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.