baculovirus dna Search Results


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(a) Detection of nitrocellulose-blotted recombinant α1-2 and α2. Supernatants from Sf9 cells infected with nonrecombinant <t>baculovirus</t> (lane 1) and from Sf9 cells infected with α1-2 (lane 2) and α2 (lane 3) recombinant baculoviruses were separated by SDS-PAGE and blotted onto nitrocellulose. Recombinant α1-2 (35 kDa) and α2 (16 kDa) are recognized by an anti-hexahistidine mAb in lanes 2 and 3, respectively. (b) Detection of nitrocellulose-blotted recombinant Cε3 with anti-human IgE antibodies. Nitrocellulose-blotted supernatants from Sf9 insect cells infected with nonrecombinant (lane 1) and Cε3III-expressing (lane 2) baculoviruses were exposed to 125I-labeled anti-human IgE antibodies.
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Biozol Diagnostica Vertrieb GmbH baculogold baculovirus dna
(a) Detection of nitrocellulose-blotted recombinant α1-2 and α2. Supernatants from Sf9 cells infected with nonrecombinant <t>baculovirus</t> (lane 1) and from Sf9 cells infected with α1-2 (lane 2) and α2 (lane 3) recombinant baculoviruses were separated by SDS-PAGE and blotted onto nitrocellulose. Recombinant α1-2 (35 kDa) and α2 (16 kDa) are recognized by an anti-hexahistidine mAb in lanes 2 and 3, respectively. (b) Detection of nitrocellulose-blotted recombinant Cε3 with anti-human IgE antibodies. Nitrocellulose-blotted supernatants from Sf9 insect cells infected with nonrecombinant (lane 1) and Cε3III-expressing (lane 2) baculoviruses were exposed to 125I-labeled anti-human IgE antibodies.
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Becton Dickinson linearized baculovirus dna transfection kit
(a) Detection of nitrocellulose-blotted recombinant α1-2 and α2. Supernatants from Sf9 cells infected with nonrecombinant <t>baculovirus</t> (lane 1) and from Sf9 cells infected with α1-2 (lane 2) and α2 (lane 3) recombinant baculoviruses were separated by SDS-PAGE and blotted onto nitrocellulose. Recombinant α1-2 (35 kDa) and α2 (16 kDa) are recognized by an anti-hexahistidine mAb in lanes 2 and 3, respectively. (b) Detection of nitrocellulose-blotted recombinant Cε3 with anti-human IgE antibodies. Nitrocellulose-blotted supernatants from Sf9 insect cells infected with nonrecombinant (lane 1) and Cε3III-expressing (lane 2) baculoviruses were exposed to 125I-labeled anti-human IgE antibodies.
Linearized Baculovirus Dna Transfection Kit, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Journal: EMBO Reports

Article Title: Monomeric agonist peptide/ MHCII complexes activate T‐cells in an autonomous fashion

doi: 10.15252/embr.202357842

Figure Lengend Snippet:

Article Snippet: BD Baculo Gold Linearized Baculovirus DNA , BD Biosciences , 554739.

Techniques: Recombinant, Sequencing, Software, Imaging, Isolation, Mutagenesis, Avidin-Biotin Assay

(a) Detection of nitrocellulose-blotted recombinant α1-2 and α2. Supernatants from Sf9 cells infected with nonrecombinant baculovirus (lane 1) and from Sf9 cells infected with α1-2 (lane 2) and α2 (lane 3) recombinant baculoviruses were separated by SDS-PAGE and blotted onto nitrocellulose. Recombinant α1-2 (35 kDa) and α2 (16 kDa) are recognized by an anti-hexahistidine mAb in lanes 2 and 3, respectively. (b) Detection of nitrocellulose-blotted recombinant Cε3 with anti-human IgE antibodies. Nitrocellulose-blotted supernatants from Sf9 insect cells infected with nonrecombinant (lane 1) and Cε3III-expressing (lane 2) baculoviruses were exposed to 125I-labeled anti-human IgE antibodies.

Journal:

Article Title: The immunoglobulin-like modules C?3 and ?2 are the minimal units necessary for human IgE-Fc?RI interaction

doi:

Figure Lengend Snippet: (a) Detection of nitrocellulose-blotted recombinant α1-2 and α2. Supernatants from Sf9 cells infected with nonrecombinant baculovirus (lane 1) and from Sf9 cells infected with α1-2 (lane 2) and α2 (lane 3) recombinant baculoviruses were separated by SDS-PAGE and blotted onto nitrocellulose. Recombinant α1-2 (35 kDa) and α2 (16 kDa) are recognized by an anti-hexahistidine mAb in lanes 2 and 3, respectively. (b) Detection of nitrocellulose-blotted recombinant Cε3 with anti-human IgE antibodies. Nitrocellulose-blotted supernatants from Sf9 insect cells infected with nonrecombinant (lane 1) and Cε3III-expressing (lane 2) baculoviruses were exposed to 125I-labeled anti-human IgE antibodies.

Article Snippet: Sf9 cells ( 24 ) were cotransfected with a mixture of the pVL1392 constructs and pAk Bac baculovirus DNA (Promega Corp., Madison, Wisconsin, USA).

Techniques: Recombinant, Infection, SDS Page, Expressing, Labeling

IgE-binding capacity of nitrocellulose-dotted, baculovirus-expressed α-chain constructs. Sf9 cell supernatants containing recombinant α1-2 (a) or α2 (b) construct were dotted on nitrocellulose. Filter-bound proteins were incubated with serum from an atopic patient containing high IgE levels (lanes 1, 4, and 5), with chimeric monoclonal IgE (2), and with a human IgE–containing myeloma supernatant (3), and were detected with 125I-labeled anti-human IgE RAST antibodies (1-3), a 125I-labeled mouse monoclonal anti-human IgE antibody 12 (4), and, for control purposes, a 125I-labeled human α chain (5).

Journal:

Article Title: The immunoglobulin-like modules C?3 and ?2 are the minimal units necessary for human IgE-Fc?RI interaction

doi:

Figure Lengend Snippet: IgE-binding capacity of nitrocellulose-dotted, baculovirus-expressed α-chain constructs. Sf9 cell supernatants containing recombinant α1-2 (a) or α2 (b) construct were dotted on nitrocellulose. Filter-bound proteins were incubated with serum from an atopic patient containing high IgE levels (lanes 1, 4, and 5), with chimeric monoclonal IgE (2), and with a human IgE–containing myeloma supernatant (3), and were detected with 125I-labeled anti-human IgE RAST antibodies (1-3), a 125I-labeled mouse monoclonal anti-human IgE antibody 12 (4), and, for control purposes, a 125I-labeled human α chain (5).

Article Snippet: Sf9 cells ( 24 ) were cotransfected with a mixture of the pVL1392 constructs and pAk Bac baculovirus DNA (Promega Corp., Madison, Wisconsin, USA).

Techniques: Binding Assay, Construct, Recombinant, Incubation, Labeling, Control