clonepix2 (Danaher Inc)
Danaher Inc is a verified supplier 
Danaher Inc manufactures this product 
94
Structured Review
Danaher Inc
clonepix2
Clonepix2, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/clonepix+2/ClonePix+2+Mammalian+Colony+Picker/us12559560-532-11-12
Average 94 stars, based on 14 article reviews
Clonepix2, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/clonepix+2/ClonePix+2+Mammalian+Colony+Picker/us12559560-532-11-12
Average 94 stars, based on 14 article reviews
clonepix2 - by Bioz Stars,
2026-09
94/100 stars
Images
Related Articles
Cytometry:Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-TMEM106B antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA) and screened for TMEM106B reactivity 5 days later.. 1205 hybridomas were obtained.1205 hybridomas were obtained. Article Title: Anti-MS4A6A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below. Article Title: An αIIbβ3 monoclonal antibody traps a semiextended conformation and allosterically inhibits large ligand binding ∗ Article Snippet: pregnated with fluorescent Fc fragment-specific antimouse IgG antibody (155-545-071, Jackson ImmunoResearch Laboratories). Single colonies were picked with the aid of a robotic instrument Western Blot:Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-TMEM106B antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA) and screened for TMEM106B reactivity 5 days later.. 1205 hybridomas were obtained.1205 hybridomas were obtained. Article Title: Anti-MS4A6A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below. Article Title: An αIIbβ3 monoclonal antibody traps a semiextended conformation and allosterically inhibits large ligand binding ∗ Article Snippet: pregnated with fluorescent Fc fragment-specific antimouse IgG antibody (155-545-071, Jackson ImmunoResearch Laboratories). Single colonies were picked with the aid of a robotic instrument Flow Cytometry:Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-TMEM106B antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA) and screened for TMEM106B reactivity 5 days later.. 1205 hybridomas were obtained.1205 hybridomas were obtained. Article Title: Anti-MS4A6A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below. Article Title: An αIIbβ3 monoclonal antibody traps a semiextended conformation and allosterically inhibits large ligand binding ∗ Article Snippet: pregnated with fluorescent Fc fragment-specific antimouse IgG antibody (155-545-071, Jackson ImmunoResearch Laboratories). Single colonies were picked with the aid of a robotic instrument Cell Culture:Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, N.Y.) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, Calif.).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-MS4A4A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below.After six days, tissue culture supernatants from the hybridomas were screened by FACS against 300.19, K562, and/or U937 cells overexpressing full length human MS4A4A, as described below. Article Title: Anti-TMEM106B antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C./5% CO2 for seven days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA) and screened for TMEM106B reactivity 5 days later.. 1205 hybridomas were obtained.1205 hybridomas were obtained. Article Title: Anti-MS4A6A antibodies and methods of use thereof Article Snippet: The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.The cells were plated into Nunc OmniTrays (Thermo Fisher Scientific, Rochester, NY) and allowed to grow at 37° C., 5% CO2 for eight days.. Fluorescent colonies were selected and transferred into 96-well plates containing Clonacell-HY Medium E (StemCell Technologies) using a Clonepix 2 (Molecular Devices, Sunnyvale, CA).. After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below.After five days, tissue culture supernatants from the hybridomas were screened by FACS against HEK293 cells overexpressing full length cyno MS4A6A as described below. Article Title: An αIIbβ3 monoclonal antibody traps a semiextended conformation and allosterically inhibits large ligand binding ∗ Article Snippet: pregnated with fluorescent Fc fragment-specific antimouse IgG antibody (155-545-071, Jackson ImmunoResearch Laboratories). Single colonies were picked with the aid of a robotic instrument |