sds page protein loading buffer Search Results


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Valiant Co Ltd protein loading buffer
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AtaGenix Inc sds-page protein loading buffer 5x
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Beijing Solarbio Science sds-page protein uploading buffer 5
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Servicebio Inc 2×sds-page loading buffer
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Yeasen Biotechnology 5 × sds-page protein loading buffer
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Bimake Inc sds protein loading buffer containing protease and phosphatase inhibitors
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Beijing Solarbio Science β-mercaptoethanol-sds protein loading buffer (4 folds volume)
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Yeasen Biotechnology sds-page protein loading buffer yeasen s3301100
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MyBiosource Biotechnology 5× sds-page protein loading buffer
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Novoprotein 5 × protein sds page loading buffer
Silver staining was used to detect the enrichment of p72 interacting proteins. A Dynamic growth of ASFVGZ in IPAM and PK-15 ​cells in vitro . IPAM or PK-15 ​cells were infected (MOI ​= ​0.1) with ASFVGZ and viral genome copies were calculated at the indicated times post-infection. PK-15 ​cells ( B ) and IPAM cells ( C ) were infected with ASFVGZ at 0.1 MOI. Anti-p72 mAb were used for CO-IP 48 ​h after cell infection. p72-interacting proteins were eluted with protein G sepharose and analyzed <t>on</t> <t>SDS-PAGE</t> followed by silver staining. The normal mouse IgG as a negative control. The data were tested three times independently. Arrows indicate differential bands.
5 × Protein Sds Page Loading Buffer, supplied by Novoprotein, 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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Silver staining was used to detect the enrichment of p72 interacting proteins. A Dynamic growth of ASFVGZ in IPAM and PK-15 ​cells in vitro . IPAM or PK-15 ​cells were infected (MOI ​= ​0.1) with ASFVGZ and viral genome copies were calculated at the indicated times post-infection. PK-15 ​cells ( B ) and IPAM cells ( C ) were infected with ASFVGZ at 0.1 MOI. Anti-p72 mAb were used for CO-IP 48 ​h after cell infection. p72-interacting proteins were eluted with protein G sepharose and analyzed on SDS-PAGE followed by silver staining. The normal mouse IgG as a negative control. The data were tested three times independently. Arrows indicate differential bands.

Journal: Virologica Sinica

Article Title: Function investigation of p11.5 in ASFV infection

doi: 10.1016/j.virs.2024.05.007

Figure Lengend Snippet: Silver staining was used to detect the enrichment of p72 interacting proteins. A Dynamic growth of ASFVGZ in IPAM and PK-15 ​cells in vitro . IPAM or PK-15 ​cells were infected (MOI ​= ​0.1) with ASFVGZ and viral genome copies were calculated at the indicated times post-infection. PK-15 ​cells ( B ) and IPAM cells ( C ) were infected with ASFVGZ at 0.1 MOI. Anti-p72 mAb were used for CO-IP 48 ​h after cell infection. p72-interacting proteins were eluted with protein G sepharose and analyzed on SDS-PAGE followed by silver staining. The normal mouse IgG as a negative control. The data were tested three times independently. Arrows indicate differential bands.

Article Snippet: The beads were washed 4 times with 1 mL phosphate-buffered saline (PBS) for 10 min, and boiled in a 5 × Protein SDS PAGE Loading Buffer (Novoprotein, Shanghai, China) for silver staining or Western blot analyses using One step PAGE Gel Fast Preparation Kit (MeilunBio, Dalian, China).

Techniques: Silver Staining, In Vitro, Infection, Co-Immunoprecipitation Assay, SDS Page, Negative Control