CIL:13569, Homo sapiens, epithelial cell, cervical carcinoma. In Cell Image Library

GalNac-T1 staining (green) colocalizes with COP-I gamma1 (red) staining at the Golgi (HPL) (gray) in unstimulated HeLa cells. Helix Pomatia Lectin (HPL) binds various glycans but the Tn antigen in particular. The Tn antigen refers to terminal α-linked N-acetyl galactosamine residues (GalNAc) linked...

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description GalNac-T1 staining (green) colocalizes with COP-I gamma1 (red) staining at the Golgi (HPL) (gray) in unstimulated HeLa cells. Helix Pomatia Lectin (HPL) binds various glycans but the Tn antigen in particular. The Tn antigen refers to terminal α-linked N-acetyl galactosamine residues (GalNAc) linked to Ser or Thr residues. HeLa cells were serum starved overnight in DME (noFBS). Cells were fixed for 10 min (4% paraformaldehyde) and permeabilized (0.2% Triton X-100). Primary antibody staining followed the manufacturer's instructions. Cells were subsequently stained for 15–30 min with secondary Alexa Fluor–conjugated antibodies (Alexa 488 for anti-GalNac-T1, Alexa 594 for anti-COP-I gamma1). Hoechst (blue) and Alexa 647-conjugated-HPL were added during secondary antibody incubations. Cells were mounted onto glass slides using FluorSave (Merck) and imaged at room temperature using an inverted FluoView confocal microscope (model IX81; Olympus) with fluorescence excitation at 488 nm, 561 nm, and 633 nm and either a 60x objective (U Plan Super Apochromatic [UPLSAPO]; NA 1.35) or 100x objective (UPLSAPO; NA 1.40) using Immersol oil. Microscope coupled with a CCD camera (model FVII). Images were acquired and processed using Olympus FV10-ASW software. Image corresponds to Fig 6E, in J Cell Biol. 189: 843-858. 2010. Images in Fig 6 include CIL#s 13563, 13564, 13565, 13566, 13567, 13568, 13569, 13570.
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Hoechst (blue) and Alexa 647-conjugated-HPL were added during secondary antibody incubations. Cells were mounted onto glass slides using FluorSave (Merck) and imaged at room temperature using an inverted FluoView confocal microscope (model IX81; Olympus) with fluorescence excitation at 488 nm, 561 nm, and 633 nm and either a 60x objective (U Plan Super Apochromatic [UPLSAPO]; NA 1.35) or 100x objective (UPLSAPO; NA 1.40) using Immersol oil. Microscope coupled with a CCD camera (model FVII). Images were acquired and processed using Olympus FV10-ASW software. Image corresponds to Fig 6E, in J Cell Biol. 189: 843-858. 2010. Images in Fig 6 include CIL#s 13563, 13564, 13565, 13566, 13567, 13568, 13569, 13570.</description><identifier>DOI: 10.6075/j0ht2n1f</identifier><language>eng</language><publisher>UC San Diego Library Digital Collections</publisher><subject>cervical carcinoma ; COPI coating of Golgi vesicle ; COPI vesicle coat ; epithelial cell ; Golgi cisterna membrane ; Golgi-associated vesicle ; HeLa ; Homo sapiens ; integral to membrane ; manganese ion binding ; N-acetylgalactosamine binding ; nucleus ; polypeptide N-acetylgalactosaminyltransferase activity ; protein binding ; protein O-linked glycosylation via serine ; protein O-linked glycosylation via threonine ; retrograde vesicle-mediated transport, Golgi to ER ; structural molecule activity</subject><creationdate>2021</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6075/j0ht2n1f$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Gill, David J.</creatorcontrib><creatorcontrib>Chia, Joanne</creatorcontrib><creatorcontrib>Senewiratne, Jamie</creatorcontrib><creatorcontrib>Bard, Frederic</creatorcontrib><title>CIL:13569, Homo sapiens, epithelial cell, cervical carcinoma. In Cell Image Library</title><description>GalNac-T1 staining (green) colocalizes with COP-I gamma1 (red) staining at the Golgi (HPL) (gray) in unstimulated HeLa cells. Helix Pomatia Lectin (HPL) binds various glycans but the Tn antigen in particular. The Tn antigen refers to terminal α-linked N-acetyl galactosamine residues (GalNAc) linked to Ser or Thr residues. HeLa cells were serum starved overnight in DME (noFBS). Cells were fixed for 10 min (4% paraformaldehyde) and permeabilized (0.2% Triton X-100). Primary antibody staining followed the manufacturer's instructions. Cells were subsequently stained for 15–30 min with secondary Alexa Fluor–conjugated antibodies (Alexa 488 for anti-GalNac-T1, Alexa 594 for anti-COP-I gamma1). Hoechst (blue) and Alexa 647-conjugated-HPL were added during secondary antibody incubations. Cells were mounted onto glass slides using FluorSave (Merck) and imaged at room temperature using an inverted FluoView confocal microscope (model IX81; Olympus) with fluorescence excitation at 488 nm, 561 nm, and 633 nm and either a 60x objective (U Plan Super Apochromatic [UPLSAPO]; NA 1.35) or 100x objective (UPLSAPO; NA 1.40) using Immersol oil. Microscope coupled with a CCD camera (model FVII). Images were acquired and processed using Olympus FV10-ASW software. Image corresponds to Fig 6E, in J Cell Biol. 189: 843-858. 2010. Images in Fig 6 include CIL#s 13563, 13564, 13565, 13566, 13567, 13568, 13569, 13570.</description><subject>cervical carcinoma</subject><subject>COPI coating of Golgi vesicle</subject><subject>COPI vesicle coat</subject><subject>epithelial cell</subject><subject>Golgi cisterna membrane</subject><subject>Golgi-associated vesicle</subject><subject>HeLa</subject><subject>Homo sapiens</subject><subject>integral to membrane</subject><subject>manganese ion binding</subject><subject>N-acetylgalactosamine binding</subject><subject>nucleus</subject><subject>polypeptide N-acetylgalactosaminyltransferase activity</subject><subject>protein binding</subject><subject>protein O-linked glycosylation via serine</subject><subject>protein O-linked glycosylation via threonine</subject><subject>retrograde vesicle-mediated transport, Golgi to ER</subject><subject>structural molecule activity</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2021</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNpjYBAwNNAzMzA31c8yyCgxyjNM42QIdvb0sTI0NjWz1FHwyM_NVyhOLMhMzSvWUUgtyCzJSM3JTMxRSE7NydEBkkVlmckgbmJRcmZefm6inoJnnoIzUFLBMzcxPVXBJzOpKLGokoeBNS0xpziVF0pzM2i4uYY4e-imJJYkJmeWpMYXFGXmAhXGGxrEg9wTD3OPMQlKAVglQFM</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Gill, David J.</creator><creator>Chia, Joanne</creator><creator>Senewiratne, Jamie</creator><creator>Bard, Frederic</creator><general>UC San Diego Library Digital Collections</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>2021</creationdate><title>CIL:13569, Homo sapiens, epithelial cell, cervical carcinoma. 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In Cell Image Library</title><date>2021</date><risdate>2021</risdate><abstract>GalNac-T1 staining (green) colocalizes with COP-I gamma1 (red) staining at the Golgi (HPL) (gray) in unstimulated HeLa cells. Helix Pomatia Lectin (HPL) binds various glycans but the Tn antigen in particular. The Tn antigen refers to terminal α-linked N-acetyl galactosamine residues (GalNAc) linked to Ser or Thr residues. HeLa cells were serum starved overnight in DME (noFBS). Cells were fixed for 10 min (4% paraformaldehyde) and permeabilized (0.2% Triton X-100). Primary antibody staining followed the manufacturer's instructions. Cells were subsequently stained for 15–30 min with secondary Alexa Fluor–conjugated antibodies (Alexa 488 for anti-GalNac-T1, Alexa 594 for anti-COP-I gamma1). Hoechst (blue) and Alexa 647-conjugated-HPL were added during secondary antibody incubations. Cells were mounted onto glass slides using FluorSave (Merck) and imaged at room temperature using an inverted FluoView confocal microscope (model IX81; Olympus) with fluorescence excitation at 488 nm, 561 nm, and 633 nm and either a 60x objective (U Plan Super Apochromatic [UPLSAPO]; NA 1.35) or 100x objective (UPLSAPO; NA 1.40) using Immersol oil. Microscope coupled with a CCD camera (model FVII). Images were acquired and processed using Olympus FV10-ASW software. Image corresponds to Fig 6E, in J Cell Biol. 189: 843-858. 2010. Images in Fig 6 include CIL#s 13563, 13564, 13565, 13566, 13567, 13568, 13569, 13570.</abstract><pub>UC San Diego Library Digital Collections</pub><doi>10.6075/j0ht2n1f</doi><oa>free_for_read</oa></addata></record>
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identifier DOI: 10.6075/j0ht2n1f
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language eng
recordid cdi_datacite_primary_10_6075_j0ht2n1f
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subjects cervical carcinoma
COPI coating of Golgi vesicle
COPI vesicle coat
epithelial cell
Golgi cisterna membrane
Golgi-associated vesicle
HeLa
Homo sapiens
integral to membrane
manganese ion binding
N-acetylgalactosamine binding
nucleus
polypeptide N-acetylgalactosaminyltransferase activity
protein binding
protein O-linked glycosylation via serine
protein O-linked glycosylation via threonine
retrograde vesicle-mediated transport, Golgi to ER
structural molecule activity
title CIL:13569, Homo sapiens, epithelial cell, cervical carcinoma. In Cell Image Library
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