3 3 diaminobenzidine dab substrate kit Search Results


human ck-3 rpa kit  (Becton Dickinson)
90
Becton Dickinson human ck-3 rpa kit
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Human Ck 3 Rpa 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
https://www.bioz.com/product/3+3+diaminobenzidine+dab+substrate+kit/pmc00111887-215-55-59?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
human ck-3 rpa kit - by Bioz Stars, 2026-08
90/100 stars
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mouse 5-ht enzyme-linked immunosorbent assay (elisa) kit  (FineTest Biotech Inc)
90
FineTest Biotech Inc mouse 5-ht enzyme-linked immunosorbent assay (elisa) kit
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Mouse 5 Ht Enzyme Linked Immunosorbent Assay (Elisa) Kit, supplied by FineTest Biotech Inc, 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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Average 90 stars, based on 1 article reviews
mouse 5-ht enzyme-linked immunosorbent assay (elisa) kit - by Bioz Stars, 2026-08
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dual rna/dna isolation kit  (Omega Bio Tek)
90
Omega Bio Tek dual rna/dna isolation kit
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Dual Rna/Dna Isolation Kit, supplied by Omega Bio Tek, 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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dual rna/dna isolation kit - by Bioz Stars, 2026-08
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dna extraction kit e.z.a tm mag-bindsoildnakit  (Omega Bio Tek)
90
Omega Bio Tek dna extraction kit e.z.a tm mag-bindsoildnakit
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Dna Extraction Kit E.Z.A Tm Mag Bindsoildnakit, supplied by Omega Bio Tek, 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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Average 90 stars, based on 1 article reviews
dna extraction kit e.z.a tm mag-bindsoildnakit - by Bioz Stars, 2026-08
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elisa kit tsh  (Beijing Solarbio Science)
90
Beijing Solarbio Science elisa kit tsh
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Elisa Kit Tsh, supplied by Beijing Solarbio Science, 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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Average 90 stars, based on 1 article reviews
elisa kit tsh - by Bioz Stars, 2026-08
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rnaseq library preparation kit mace v1.0  (GenXPro Inc)
90
GenXPro Inc rnaseq library preparation kit mace v1.0
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Rnaseq Library Preparation Kit Mace V1.0, supplied by GenXPro Inc, 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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Average 90 stars, based on 1 article reviews
rnaseq library preparation kit mace v1.0 - by Bioz Stars, 2026-08
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mounting medium merifluor giardia and cryptosporidium kit  (Meridian Bioscience)
90
Meridian Bioscience mounting medium merifluor giardia and cryptosporidium kit
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Mounting Medium Merifluor Giardia And Cryptosporidium Kit, supplied by Meridian Bioscience, 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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Average 90 stars, based on 1 article reviews
mounting medium merifluor giardia and cryptosporidium kit - by Bioz Stars, 2026-08
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bad shrnas  (OriGene)
90
OriGene bad shrnas
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Bad Shrnas, supplied by OriGene, 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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Average 90 stars, based on 1 article reviews
bad shrnas - by Bioz Stars, 2026-08
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quantseq 3' mrna-seq library prep kit rev  (Lexogen GmbH)
90
Lexogen GmbH quantseq 3' mrna-seq library prep kit rev
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Quantseq 3' Mrna Seq Library Prep Kit Rev, supplied by Lexogen GmbH, 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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quantseq 3' mrna-seq library prep kit rev - by Bioz Stars, 2026-08
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native barcode expansion kit exp-nbd103 (barcode 3)  (Oxford Nanopore)
90
Oxford Nanopore native barcode expansion kit exp-nbd103 (barcode 3)
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Native Barcode Expansion Kit Exp Nbd103 (Barcode 3), supplied by Oxford Nanopore, 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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native barcode expansion kit exp-nbd103 (barcode 3) - by Bioz Stars, 2026-08
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epiquik total histone extraction kit  (EpiGentek)
90
EpiGentek epiquik total histone extraction kit
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Epiquik Total Histone Extraction Kit, supplied by EpiGentek, 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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epiquik total histone extraction kit - by Bioz Stars, 2026-08
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truseq rna sample prep kit v2  (Illumina Inc)
99
Illumina Inc truseq rna sample prep kit v2
IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) <t>RPA</t> of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human <t>CK-3</t> RPA kit (Pharmingen), according to manufacturer's instructions.
Truseq Rna Sample Prep Kit V2, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) RPA of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human CK-3 RPA kit (Pharmingen), according to manufacturer's instructions.

Journal:

Article Title: The IRF-3 Transcription Factor Mediates Sendai Virus-Induced Apoptosis

doi:

Figure Lengend Snippet: IFN release is not implicated in IRF-3-induced apoptosis. (A) Control 293 and 293 IRF-3 ΔN-expressing cells were left untreated or were infected with Sendai virus (80 HAU/ml) for 24, 48, and 72 h in the presence or absence of IFN-α (400 IU/ml) or neutralizing antibody for alpha/beta interferon (1/100) (Sigma) as indicated. Viability was measured by using an MTT assay as described in Materials and Methods. Symbols: ■, 293; □, 293 plus IFN-α; ▵, 293 plus anti-IFN-α; ●, 293 IRF-3 ΔN. (B) TUNEL staining of Jurkat cells. The rtTA-Jurkat cells were either left untreated, were infected with Sendai virus (80 HAU/ml), or were treated with IFN-α (400 IU/ml) for 72 h; anti-IFN-α antibody was added with Sendai virus. The number of apoptotic cells was determined by TUNEL as described in Materials and Methods. (C) RPA of IFN-β and IFN-γ mRNA production. The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human CK-3 RPA kit (Pharmingen), according to manufacturer's instructions.

Article Snippet: The rtTA-, wtIRF-3-, and IRF-3(5D)-expressing 293 and Jurkat cells were cultured in the presence or absence of DOX, as indicated, for 24 h. Cells were then either left untreated or were infected with Sendai virus for 72 h. Total RNA was isolated from each sample and was analyzed by RNase protection analysis by using the human CK-3 RPA kit (Pharmingen), according to manufacturer's instructions.

Techniques: Expressing, Infection, MTT Assay, TUNEL Assay, Staining, Cell Culture, Isolation