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u2os egfp dcp1a ugd stable line  (ATCC)


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    Structured Review

    ATCC u2os egfp dcp1a ugd stable line
    U2os Egfp Dcp1a Ugd Stable Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 2502 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/egfp+2/U-2+OS/pm41877182-161-15-12
    Average 98 stars, based on 2502 article reviews
    u2os egfp dcp1a ugd stable line - by Bioz Stars, 2026-09
    98/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Plants with increased photorespiration efficiency
    Article Snippet: .. TABLE 2 Plasmids Plasmid Inserted genes Promoter Vector Source EC50505 none EC50505 ENSA (project ensa.ac.uk) EC27349 p19, eGFP 2 × 35 s EC50505 This study EC27357 p19, BASS6- 2 × 35 s EC50505 This study eGFP p415 none p415 ATCC-87374 ADH1 ADH1 BASS6 ADH1 p415 This study ADH1 PLGG1 ADH1 p415 This study ADH1 EC15325 BAR NOS EC50505 ENSA (project ensa.ac.uk) EC27403 BAR, PLGG1 NOS, PLGG1 EC15325 This study EC27404 BAR, BASS6 NOS, BASS6 EC15325 This study EC27406 BAR, BASS6 NOS, PLGG1 EC15325 This study For the transient expression work on isolated protoplasts, the BASS6-GFP construct was cloned as follows. .. The coding sequence of A. thaliana Bass6 (AT4G22840) was synthesized by GENEWIZ Inc. with a C-terminal tag containing mGFP6 (Haseloff, J., Method Cell Biol. (1999) 58:139-51), 6×HIS and MYC, into a modified gateway-compatible pUC57 plasmid from which it was recombined in pMDC32.

    Expressing:

    Article Title: Plants with increased photorespiration efficiency
    Article Snippet: .. TABLE 2 Plasmids Plasmid Inserted genes Promoter Vector Source EC50505 none EC50505 ENSA (project ensa.ac.uk) EC27349 p19, eGFP 2 × 35 s EC50505 This study EC27357 p19, BASS6- 2 × 35 s EC50505 This study eGFP p415 none p415 ATCC-87374 ADH1 ADH1 BASS6 ADH1 p415 This study ADH1 PLGG1 ADH1 p415 This study ADH1 EC15325 BAR NOS EC50505 ENSA (project ensa.ac.uk) EC27403 BAR, PLGG1 NOS, PLGG1 EC15325 This study EC27404 BAR, BASS6 NOS, BASS6 EC15325 This study EC27406 BAR, BASS6 NOS, PLGG1 EC15325 This study For the transient expression work on isolated protoplasts, the BASS6-GFP construct was cloned as follows. .. The coding sequence of A. thaliana Bass6 (AT4G22840) was synthesized by GENEWIZ Inc. with a C-terminal tag containing mGFP6 (Haseloff, J., Method Cell Biol. (1999) 58:139-51), 6×HIS and MYC, into a modified gateway-compatible pUC57 plasmid from which it was recombined in pMDC32.

    Isolation:

    Article Title: Plants with increased photorespiration efficiency
    Article Snippet: .. TABLE 2 Plasmids Plasmid Inserted genes Promoter Vector Source EC50505 none EC50505 ENSA (project ensa.ac.uk) EC27349 p19, eGFP 2 × 35 s EC50505 This study EC27357 p19, BASS6- 2 × 35 s EC50505 This study eGFP p415 none p415 ATCC-87374 ADH1 ADH1 BASS6 ADH1 p415 This study ADH1 PLGG1 ADH1 p415 This study ADH1 EC15325 BAR NOS EC50505 ENSA (project ensa.ac.uk) EC27403 BAR, PLGG1 NOS, PLGG1 EC15325 This study EC27404 BAR, BASS6 NOS, BASS6 EC15325 This study EC27406 BAR, BASS6 NOS, PLGG1 EC15325 This study For the transient expression work on isolated protoplasts, the BASS6-GFP construct was cloned as follows. .. The coding sequence of A. thaliana Bass6 (AT4G22840) was synthesized by GENEWIZ Inc. with a C-terminal tag containing mGFP6 (Haseloff, J., Method Cell Biol. (1999) 58:139-51), 6×HIS and MYC, into a modified gateway-compatible pUC57 plasmid from which it was recombined in pMDC32.

    Construct:

    Article Title: Plants with increased photorespiration efficiency
    Article Snippet: .. TABLE 2 Plasmids Plasmid Inserted genes Promoter Vector Source EC50505 none EC50505 ENSA (project ensa.ac.uk) EC27349 p19, eGFP 2 × 35 s EC50505 This study EC27357 p19, BASS6- 2 × 35 s EC50505 This study eGFP p415 none p415 ATCC-87374 ADH1 ADH1 BASS6 ADH1 p415 This study ADH1 PLGG1 ADH1 p415 This study ADH1 EC15325 BAR NOS EC50505 ENSA (project ensa.ac.uk) EC27403 BAR, PLGG1 NOS, PLGG1 EC15325 This study EC27404 BAR, BASS6 NOS, BASS6 EC15325 This study EC27406 BAR, BASS6 NOS, PLGG1 EC15325 This study For the transient expression work on isolated protoplasts, the BASS6-GFP construct was cloned as follows. .. The coding sequence of A. thaliana Bass6 (AT4G22840) was synthesized by GENEWIZ Inc. with a C-terminal tag containing mGFP6 (Haseloff, J., Method Cell Biol. (1999) 58:139-51), 6×HIS and MYC, into a modified gateway-compatible pUC57 plasmid from which it was recombined in pMDC32.

    Clone Assay:

    Article Title: Plants with increased photorespiration efficiency
    Article Snippet: .. TABLE 2 Plasmids Plasmid Inserted genes Promoter Vector Source EC50505 none EC50505 ENSA (project ensa.ac.uk) EC27349 p19, eGFP 2 × 35 s EC50505 This study EC27357 p19, BASS6- 2 × 35 s EC50505 This study eGFP p415 none p415 ATCC-87374 ADH1 ADH1 BASS6 ADH1 p415 This study ADH1 PLGG1 ADH1 p415 This study ADH1 EC15325 BAR NOS EC50505 ENSA (project ensa.ac.uk) EC27403 BAR, PLGG1 NOS, PLGG1 EC15325 This study EC27404 BAR, BASS6 NOS, BASS6 EC15325 This study EC27406 BAR, BASS6 NOS, PLGG1 EC15325 This study For the transient expression work on isolated protoplasts, the BASS6-GFP construct was cloned as follows. .. The coding sequence of A. thaliana Bass6 (AT4G22840) was synthesized by GENEWIZ Inc. with a C-terminal tag containing mGFP6 (Haseloff, J., Method Cell Biol. (1999) 58:139-51), 6×HIS and MYC, into a modified gateway-compatible pUC57 plasmid from which it was recombined in pMDC32.



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    (a) Lysates from HEK293T cells transiently expressing the indicated proteins (top) were subjected to immunoprecipitation <t>with</t> <t>anti-EGFP</t> beads (IP: EGFP). Immunoprecipitates (IPs) and lysates were then analyzed by Western blot (WB) with antibodies against phosphotyrosine (pY), EGFP, Flag or active SRC (SRC pY419). (b) Similar experiment as in (a), except INPP5E was expressed with a Flag epitope and immunoprecipitated with anti-Flag beads (IP: Flag), while the other proteins were expressed as EGFP fusions. Molecular weight markers are shown on the right (kDa). Note how pY signal in (b) matches size of Flag-INPP5E (≈73 kDa), whereas in (a) it matches that of EGFP-INPP5E (≈100 kDa).
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    (a) Lysates from HEK293T cells transiently expressing the indicated proteins (top) were subjected to immunoprecipitation <t>with</t> <t>anti-EGFP</t> beads (IP: EGFP). Immunoprecipitates (IPs) and lysates were then analyzed by Western blot (WB) with antibodies against phosphotyrosine (pY), EGFP, Flag or active SRC (SRC pY419). (b) Similar experiment as in (a), except INPP5E was expressed with a Flag epitope and immunoprecipitated with anti-Flag beads (IP: Flag), while the other proteins were expressed as EGFP fusions. Molecular weight markers are shown on the right (kDa). Note how pY signal in (b) matches size of Flag-INPP5E (≈73 kDa), whereas in (a) it matches that of EGFP-INPP5E (≈100 kDa).
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    Image Search Results


    (a) Lysates from HEK293T cells transiently expressing the indicated proteins (top) were subjected to immunoprecipitation with anti-EGFP beads (IP: EGFP). Immunoprecipitates (IPs) and lysates were then analyzed by Western blot (WB) with antibodies against phosphotyrosine (pY), EGFP, Flag or active SRC (SRC pY419). (b) Similar experiment as in (a), except INPP5E was expressed with a Flag epitope and immunoprecipitated with anti-Flag beads (IP: Flag), while the other proteins were expressed as EGFP fusions. Molecular weight markers are shown on the right (kDa). Note how pY signal in (b) matches size of Flag-INPP5E (≈73 kDa), whereas in (a) it matches that of EGFP-INPP5E (≈100 kDa).

    Journal: bioRxiv

    Article Title: INPP5E interactome reveals novel connections to growth factor signaling

    doi: 10.64898/2026.02.13.705725

    Figure Lengend Snippet: (a) Lysates from HEK293T cells transiently expressing the indicated proteins (top) were subjected to immunoprecipitation with anti-EGFP beads (IP: EGFP). Immunoprecipitates (IPs) and lysates were then analyzed by Western blot (WB) with antibodies against phosphotyrosine (pY), EGFP, Flag or active SRC (SRC pY419). (b) Similar experiment as in (a), except INPP5E was expressed with a Flag epitope and immunoprecipitated with anti-Flag beads (IP: Flag), while the other proteins were expressed as EGFP fusions. Molecular weight markers are shown on the right (kDa). Note how pY signal in (b) matches size of Flag-INPP5E (≈73 kDa), whereas in (a) it matches that of EGFP-INPP5E (≈100 kDa).

    Article Snippet: Mouse anti-alpha-tubulin (Proteintech, 66031-1-Ig), mouse anti-EGFP (Proteintech, 66002-1-Ig), rabbit anti-EGFP (Proteintech, 50430-2-AP), mouse anti-Flag (Proteintech, 66008-3-Ig, or Sigma, F3165 or F1804), rabbit anti-Myc (Proteintech, 16286-1-AP) and mouse anti-V5 (Thermofisher, MA5-15253) were used as described [ , ].

    Techniques: Expressing, Immunoprecipitation, Western Blot, FLAG-tag, Molecular Weight

    (a) PI(4,5)P 2 phosphatase activity assay was performed on anti-EGFP immunoprecipitates from HEK293T cell lysates cotransfected with EGFP-INPP5E and PDGFRα-Flag (WT or D842V), as indicated. EGFP-INPP5E WT and D477N (catalytically inactive mutant) were used as positive and negative controls, respectively. Data are mean±SD of n=3 technical replicates from a single experiment. (b) Same as in (a) but using PIP 3 as substrate for the phosphatase activity assay. The INPP5E-catalyzed 5-phosphatase reactions are shown above for both substrates.

    Journal: bioRxiv

    Article Title: INPP5E interactome reveals novel connections to growth factor signaling

    doi: 10.64898/2026.02.13.705725

    Figure Lengend Snippet: (a) PI(4,5)P 2 phosphatase activity assay was performed on anti-EGFP immunoprecipitates from HEK293T cell lysates cotransfected with EGFP-INPP5E and PDGFRα-Flag (WT or D842V), as indicated. EGFP-INPP5E WT and D477N (catalytically inactive mutant) were used as positive and negative controls, respectively. Data are mean±SD of n=3 technical replicates from a single experiment. (b) Same as in (a) but using PIP 3 as substrate for the phosphatase activity assay. The INPP5E-catalyzed 5-phosphatase reactions are shown above for both substrates.

    Article Snippet: Mouse anti-alpha-tubulin (Proteintech, 66031-1-Ig), mouse anti-EGFP (Proteintech, 66002-1-Ig), rabbit anti-EGFP (Proteintech, 50430-2-AP), mouse anti-Flag (Proteintech, 66008-3-Ig, or Sigma, F3165 or F1804), rabbit anti-Myc (Proteintech, 16286-1-AP) and mouse anti-V5 (Thermofisher, MA5-15253) were used as described [ , ].

    Techniques: Phosphatase Assay, Mutagenesis

    (a) Lysates from HEK293T cells transiently expressing the indicated EGFP fusion proteins (top) and treated or not with orthovanadate, a tyrosine phosphatase inhibitor, were immunoprecipitated with anti-EGFP beads (IP: EGFP) and analyzed by Western blot (WB) with anti-phosphotyrosine (pY) and anti-EGFP antibodies, as indicated. Molecular weight markers on the right (kDa).

    Journal: bioRxiv

    Article Title: INPP5E interactome reveals novel connections to growth factor signaling

    doi: 10.64898/2026.02.13.705725

    Figure Lengend Snippet: (a) Lysates from HEK293T cells transiently expressing the indicated EGFP fusion proteins (top) and treated or not with orthovanadate, a tyrosine phosphatase inhibitor, were immunoprecipitated with anti-EGFP beads (IP: EGFP) and analyzed by Western blot (WB) with anti-phosphotyrosine (pY) and anti-EGFP antibodies, as indicated. Molecular weight markers on the right (kDa).

    Article Snippet: Mouse anti-alpha-tubulin (Proteintech, 66031-1-Ig), mouse anti-EGFP (Proteintech, 66002-1-Ig), rabbit anti-EGFP (Proteintech, 50430-2-AP), mouse anti-Flag (Proteintech, 66008-3-Ig, or Sigma, F3165 or F1804), rabbit anti-Myc (Proteintech, 16286-1-AP) and mouse anti-V5 (Thermofisher, MA5-15253) were used as described [ , ].

    Techniques: Expressing, Immunoprecipitation, Western Blot, Molecular Weight

    (a) Lysates from HEK293T cells transiently expressing the indicated proteins (top) were subjected to immunoprecipitation with anti-EGFP beads (IP: EGFP). Immunoprecipitates (IPs) and lysates were then analyzed by Western blot (WB) with antibodies against phosphotyrosine (pY), EGFP, Flag or active SRC (SRC pY419). (b) Similar experiment as in (a), except INPP5E was expressed with a Flag epitope and immunoprecipitated with anti-Flag beads (IP: Flag), while the other proteins were expressed as EGFP fusions. Molecular weight markers are shown on the right (kDa). Note how pY signal in (b) matches size of Flag-INPP5E (≈73 kDa), whereas in (a) it matches that of EGFP-INPP5E (≈100 kDa).

    Journal: bioRxiv

    Article Title: INPP5E interactome reveals novel connections to growth factor signaling

    doi: 10.64898/2026.02.13.705725

    Figure Lengend Snippet: (a) Lysates from HEK293T cells transiently expressing the indicated proteins (top) were subjected to immunoprecipitation with anti-EGFP beads (IP: EGFP). Immunoprecipitates (IPs) and lysates were then analyzed by Western blot (WB) with antibodies against phosphotyrosine (pY), EGFP, Flag or active SRC (SRC pY419). (b) Similar experiment as in (a), except INPP5E was expressed with a Flag epitope and immunoprecipitated with anti-Flag beads (IP: Flag), while the other proteins were expressed as EGFP fusions. Molecular weight markers are shown on the right (kDa). Note how pY signal in (b) matches size of Flag-INPP5E (≈73 kDa), whereas in (a) it matches that of EGFP-INPP5E (≈100 kDa).

    Article Snippet: Mouse anti-alpha-tubulin (Proteintech, 66031-1-Ig), mouse anti-EGFP (Proteintech, 66002-1-Ig), rabbit anti-EGFP (Proteintech, 50430-2-AP), mouse anti-Flag (Proteintech, 66008-3-Ig, or Sigma, F3165 or F1804), rabbit anti-Myc (Proteintech, 16286-1-AP) and mouse anti-V5 (Thermofisher, MA5-15253) were used as described [ , ].

    Techniques: Expressing, Immunoprecipitation, Western Blot, FLAG-tag, Molecular Weight

    (a) PI(4,5)P 2 phosphatase activity assay was performed on anti-EGFP immunoprecipitates from HEK293T cell lysates cotransfected with EGFP-INPP5E and PDGFRα-Flag (WT or D842V), as indicated. EGFP-INPP5E WT and D477N (catalytically inactive mutant) were used as positive and negative controls, respectively. Data are mean±SD of n=3 technical replicates from a single experiment. (b) Same as in (a) but using PIP 3 as substrate for the phosphatase activity assay. The INPP5E-catalyzed 5-phosphatase reactions are shown above for both substrates.

    Journal: bioRxiv

    Article Title: INPP5E interactome reveals novel connections to growth factor signaling

    doi: 10.64898/2026.02.13.705725

    Figure Lengend Snippet: (a) PI(4,5)P 2 phosphatase activity assay was performed on anti-EGFP immunoprecipitates from HEK293T cell lysates cotransfected with EGFP-INPP5E and PDGFRα-Flag (WT or D842V), as indicated. EGFP-INPP5E WT and D477N (catalytically inactive mutant) were used as positive and negative controls, respectively. Data are mean±SD of n=3 technical replicates from a single experiment. (b) Same as in (a) but using PIP 3 as substrate for the phosphatase activity assay. The INPP5E-catalyzed 5-phosphatase reactions are shown above for both substrates.

    Article Snippet: Mouse anti-alpha-tubulin (Proteintech, 66031-1-Ig), mouse anti-EGFP (Proteintech, 66002-1-Ig), rabbit anti-EGFP (Proteintech, 50430-2-AP), mouse anti-Flag (Proteintech, 66008-3-Ig, or Sigma, F3165 or F1804), rabbit anti-Myc (Proteintech, 16286-1-AP) and mouse anti-V5 (Thermofisher, MA5-15253) were used as described [ , ].

    Techniques: Phosphatase Assay, Mutagenesis

    (a) Lysates from HEK293T cells transiently expressing the indicated EGFP fusion proteins (top) and treated or not with orthovanadate, a tyrosine phosphatase inhibitor, were immunoprecipitated with anti-EGFP beads (IP: EGFP) and analyzed by Western blot (WB) with anti-phosphotyrosine (pY) and anti-EGFP antibodies, as indicated. Molecular weight markers on the right (kDa).

    Journal: bioRxiv

    Article Title: INPP5E interactome reveals novel connections to growth factor signaling

    doi: 10.64898/2026.02.13.705725

    Figure Lengend Snippet: (a) Lysates from HEK293T cells transiently expressing the indicated EGFP fusion proteins (top) and treated or not with orthovanadate, a tyrosine phosphatase inhibitor, were immunoprecipitated with anti-EGFP beads (IP: EGFP) and analyzed by Western blot (WB) with anti-phosphotyrosine (pY) and anti-EGFP antibodies, as indicated. Molecular weight markers on the right (kDa).

    Article Snippet: Mouse anti-alpha-tubulin (Proteintech, 66031-1-Ig), mouse anti-EGFP (Proteintech, 66002-1-Ig), rabbit anti-EGFP (Proteintech, 50430-2-AP), mouse anti-Flag (Proteintech, 66008-3-Ig, or Sigma, F3165 or F1804), rabbit anti-Myc (Proteintech, 16286-1-AP) and mouse anti-V5 (Thermofisher, MA5-15253) were used as described [ , ].

    Techniques: Expressing, Immunoprecipitation, Western Blot, Molecular Weight