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Amaxa nucleofector ii machine
Nucleofector Ii Machine, supplied by Amaxa, 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/nucleofector+ii+machine/nucleofector/pmc11536159__pnas__2416097121__sapp-107-19-18
Average 90 stars, based on 1 article reviews
nucleofector ii machine - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

Transfection:

Article Title: Methods and compositions for increasing the suppressive function of regulatory T-cells (Tregs)
Article Snippet: .. Cuvettes were loaded into the Amaxa Nucleofector II machine and transfected using Nucleofector Program X-001 for mouse CD4 T-cells. .. After transfection, the transfer pipettes provided by Amaxa were used to mix about 200-300 μL of warmed media with the cell solution in the cuvette, and the cells were gently transferred into a 12 well plate.

Article Title: A calibrated cell-based functional assay to aide classification of MLH1 DNA mismatch repair gene variants
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously with the following modifications: a ribonucleoprotein (RNP)-based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre-incubated with the variant-specific Alt-R sgRNAs/crRNAs as per manufacturer’s recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/mL puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Article Title: A calibrated cell-based functional assay to aid classification of MLH1 DNA mismatch repair gene variants.
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously (Rath et al., 2019) with the following modifications: a ribonucleoprotein (RNP)‐based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre‐incubated with the variant‐ specific Alt‐R sgRNAs/crRNAs as per manufacturer's recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/ml puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Suspension:

Article Title:
Article Snippet: For electroporation assays, 2x106 SUDHL-4 cells were used 220 in a final volume of 100μL Nucleofector Solution V with supplement (Lonza) and 2μg pcDNA3.1 221 plasmid encoding EBV antigen(s) as indicated in text. .. The cell suspension was added to a 2mm 222 gap sterile cuvette, and electroporation was performed using an Amaxa Nucleofector II machine 223 with program O-006. .. After electroporation, cells were immediately transferred to 1.5mL freshly 224 warmed LymphoONE Xeno-Free Medium (Takara Bio) in a 6-well plate and incubated for 16hrs.

Sterility:

Article Title:
Article Snippet: For electroporation assays, 2x106 SUDHL-4 cells were used 220 in a final volume of 100μL Nucleofector Solution V with supplement (Lonza) and 2μg pcDNA3.1 221 plasmid encoding EBV antigen(s) as indicated in text. .. The cell suspension was added to a 2mm 222 gap sterile cuvette, and electroporation was performed using an Amaxa Nucleofector II machine 223 with program O-006. .. After electroporation, cells were immediately transferred to 1.5mL freshly 224 warmed LymphoONE Xeno-Free Medium (Takara Bio) in a 6-well plate and incubated for 16hrs.

Electroporation:

Article Title:
Article Snippet: For electroporation assays, 2x106 SUDHL-4 cells were used 220 in a final volume of 100μL Nucleofector Solution V with supplement (Lonza) and 2μg pcDNA3.1 221 plasmid encoding EBV antigen(s) as indicated in text. .. The cell suspension was added to a 2mm 222 gap sterile cuvette, and electroporation was performed using an Amaxa Nucleofector II machine 223 with program O-006. .. After electroporation, cells were immediately transferred to 1.5mL freshly 224 warmed LymphoONE Xeno-Free Medium (Takara Bio) in a 6-well plate and incubated for 16hrs.

other:

Article Title: The ER tether VAPA is required for proper cell motility and anchors ER-PM contact sites to focal adhesions
Article Snippet: For each transfection, 0.5 million Caco2 cells were nucleofected with 2 μg of DNA in 100 μL of T solution using the B024 program on Amaxa Nuclefector II machine, as recommended by the manufacturer (Lonza).

Selection:

Article Title: A calibrated cell-based functional assay to aide classification of MLH1 DNA mismatch repair gene variants
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously with the following modifications: a ribonucleoprotein (RNP)-based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre-incubated with the variant-specific Alt-R sgRNAs/crRNAs as per manufacturer’s recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/mL puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Article Title: A calibrated cell-based functional assay to aid classification of MLH1 DNA mismatch repair gene variants.
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously (Rath et al., 2019) with the following modifications: a ribonucleoprotein (RNP)‐based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre‐incubated with the variant‐ specific Alt‐R sgRNAs/crRNAs as per manufacturer's recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/ml puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Single Cell:

Article Title: A calibrated cell-based functional assay to aide classification of MLH1 DNA mismatch repair gene variants
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously with the following modifications: a ribonucleoprotein (RNP)-based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre-incubated with the variant-specific Alt-R sgRNAs/crRNAs as per manufacturer’s recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/mL puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Article Title: A calibrated cell-based functional assay to aid classification of MLH1 DNA mismatch repair gene variants.
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously (Rath et al., 2019) with the following modifications: a ribonucleoprotein (RNP)‐based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre‐incubated with the variant‐ specific Alt‐R sgRNAs/crRNAs as per manufacturer's recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/ml puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Clone Assay:

Article Title: A calibrated cell-based functional assay to aide classification of MLH1 DNA mismatch repair gene variants
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously with the following modifications: a ribonucleoprotein (RNP)-based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre-incubated with the variant-specific Alt-R sgRNAs/crRNAs as per manufacturer’s recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/mL puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.

Article Title: A calibrated cell-based functional assay to aid classification of MLH1 DNA mismatch repair gene variants.
Article Snippet: Homozygous insertion of the given single nucleotide variant was performed as described previously (Rath et al., 2019) with the following modifications: a ribonucleoprotein (RNP)‐based targeting approach was used with either a Cas9 or Cas12a recombinant enzyme pre‐incubated with the variant‐ specific Alt‐R sgRNAs/crRNAs as per manufacturer's recommendations (IDT). .. Following transfection with the Amaxa Stem Cell Nucleofector Kit 2 (Lonza) using an Amaxa Nucleofector II machine, cells underwent selection with 1 μg/ml puromycin (Sigma) for a period of 48 h to isolate single cell clones. .. Surviving cells were treated with CloneR (STEMCELL Technologies) as recommended.



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