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Structured Review

Addgene inc px260
Px260, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 54 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px260+plasmid/pX260-U6-DR-BB-DR-Cbh-NLS-hSpCas9-NLS-H1-shorttracr-PGK-puro+(Plasmid+%2342229)/pm41803672-487-31-32
Average 93 stars, based on 54 article reviews
px260 - by Bioz Stars, 2026-09
93/100 stars

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Related Articles

Amplification:

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD-401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

Article Title: Rapid generation and selection of Cas9-engineering TRP53 R172P mice that do not have off-target effects
Article Snippet: .. The Cas9- coding region was PCR amplified with Phusion DNA polymerase from the pX260 plasmid (Addgene) using the Cas9-F primer containing the T7 promoter and Cas9-R primer (Additional file : Data 1). ..

Plasmid Preparation:

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD-401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

Article Title: Beta-2 microglobulin knockout K562 cell-based artificial antigen presenting cells for ex vivo expansion of T lymphocytes.
Article Snippet: Aim: The human K562 leukemia cell line as a scaffold of artificial antigen presenting cells (aAPCs) for ex vivo lymphocyte expansion does not usually express major histocompatibility complex (MHC) molecules.. However, when stimulated by supernatants from human T lymphocyte cultures, K562 cells upregulate β-2 microglobulin (B2M) and MHC class I expression, which would induce allo-specific T cells.. Methods: We disrupted the B2M locus in K562 cells by CRISPR/Cas9 and achieved MHC class I-negative K562 cells.

Article Title: A small-molecule lycorine derivative reveals Na + /K + -ATPase α3 as an anti-obesity target
Article Snippet: IC 50 was calculated by Graphpad Prism 7. .. The T7 promoter sequence was fused with the Cas9 coding region which was cloned from pX260 plasmid (Addgene #42229). .. Similarly, T7 promoter sequence and the targeting sequence of ATP1A1 and ATP1A3 were fused to the guide RNA scaffold which was cloned from pX330 plasmid (Addgene # 42230).

Article Title: Mycobacterium tuberculosis inhibits METTL14-mediated m 6 A methylation of Nox2 mRNA and suppresses anti-TB immunity
Article Snippet: .. The T7 promoter sequence was fused with the Cas9 coding region which was cloned from pX260 plasmid (Addgene #42229). .. Similarly, the T7 promoter sequence and the targeting sequence of STING were fused to the guide RNA scaffold which was cloned from the pX330 plasmid (Addgene # 42230).

Article Title: TAK1 is an essential kinase for STING trafficking.
Article Snippet: Article

Article Title: Rapid generation and selection of Cas9-engineering TRP53 R172P mice that do not have off-target effects
Article Snippet: .. The Cas9- coding region was PCR amplified with Phusion DNA polymerase from the pX260 plasmid (Addgene) using the Cas9-F primer containing the T7 promoter and Cas9-R primer (Additional file : Data 1). ..

Purification:

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD-401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

DNA Purification:

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

Article Title: MGA loss-of-function variants cause premature ovarian insufficiency
Article Snippet: .. Cas9 was amplified from the pX260 plasmid (Addgene) using KOD-Plus-Neo (KOD-401, TOYOBO) and purified using the Universal DNA Purification Kit (DP214, TIANGEN). .. The purified Cas9 was then transcribed in vitro using the mMESSAGE mMACHINE T7 ULTRA Kit (AM1345, Life Technologies).

CRISPR:

Article Title: Beta-2 microglobulin knockout K562 cell-based artificial antigen presenting cells for ex vivo expansion of T lymphocytes.
Article Snippet: Aim: The human K562 leukemia cell line as a scaffold of artificial antigen presenting cells (aAPCs) for ex vivo lymphocyte expansion does not usually express major histocompatibility complex (MHC) molecules.. However, when stimulated by supernatants from human T lymphocyte cultures, K562 cells upregulate β-2 microglobulin (B2M) and MHC class I expression, which would induce allo-specific T cells.. Methods: We disrupted the B2M locus in K562 cells by CRISPR/Cas9 and achieved MHC class I-negative K562 cells.

Sequencing:

Article Title: A small-molecule lycorine derivative reveals Na + /K + -ATPase α3 as an anti-obesity target
Article Snippet: IC 50 was calculated by Graphpad Prism 7. .. The T7 promoter sequence was fused with the Cas9 coding region which was cloned from pX260 plasmid (Addgene #42229). .. Similarly, T7 promoter sequence and the targeting sequence of ATP1A1 and ATP1A3 were fused to the guide RNA scaffold which was cloned from pX330 plasmid (Addgene # 42230).

Article Title: Mycobacterium tuberculosis inhibits METTL14-mediated m 6 A methylation of Nox2 mRNA and suppresses anti-TB immunity
Article Snippet: .. The T7 promoter sequence was fused with the Cas9 coding region which was cloned from pX260 plasmid (Addgene #42229). .. Similarly, the T7 promoter sequence and the targeting sequence of STING were fused to the guide RNA scaffold which was cloned from the pX330 plasmid (Addgene # 42230).

Clone Assay:

Article Title: A small-molecule lycorine derivative reveals Na + /K + -ATPase α3 as an anti-obesity target
Article Snippet: IC 50 was calculated by Graphpad Prism 7. .. The T7 promoter sequence was fused with the Cas9 coding region which was cloned from pX260 plasmid (Addgene #42229). .. Similarly, T7 promoter sequence and the targeting sequence of ATP1A1 and ATP1A3 were fused to the guide RNA scaffold which was cloned from pX330 plasmid (Addgene # 42230).

Article Title: Mycobacterium tuberculosis inhibits METTL14-mediated m 6 A methylation of Nox2 mRNA and suppresses anti-TB immunity
Article Snippet: .. The T7 promoter sequence was fused with the Cas9 coding region which was cloned from pX260 plasmid (Addgene #42229). .. Similarly, the T7 promoter sequence and the targeting sequence of STING were fused to the guide RNA scaffold which was cloned from the pX330 plasmid (Addgene # 42230).

Article Title: TAK1 is an essential kinase for STING trafficking.
Article Snippet: Article

other:

Article Title: Cytoplasmic PARP1 links the genome instability to the inhibition of antiviral immunity through PARylating cGAS.
Article Snippet: Similarly, T7 promoter sequence and the targeting sequence of cGASwere fused to the guide RNA scaffold whichwas cloned from pX330 plasmid (Addgene # 42230).

Polymerase Chain Reaction:

Article Title: Rapid generation and selection of Cas9-engineering TRP53 R172P mice that do not have off-target effects
Article Snippet: .. The Cas9- coding region was PCR amplified with Phusion DNA polymerase from the pX260 plasmid (Addgene) using the Cas9-F primer containing the T7 promoter and Cas9-R primer (Additional file : Data 1). ..



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