cell culture ramos cells Search Results


90
China Center for Type Culture Collection ramos cell line
Ramos Cell Line, supplied by China Center for Type Culture Collection, 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/result/ramos cell line/product/China Center for Type Culture Collection
Average 90 stars, based on 1 article reviews
ramos cell line - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

90
China Center for Type Culture Collection human leukemia cell ramos
In vitro test on the specificity and stability of Sgc8. ( A ) Binding ability <t>to</t> <t>HCT116</t> cells and <t>Ramos</t> cells tested with flow cytometric assay. Unmodified Sgc8 was used as the positive control, and library (lib) was used as the negative control. The cells were incubated with DNAs respectively at a concentration of 250 nM in a binding buffer for 30 min. The incubation temperature was 4°C. ( B ) Stability of Sgc8 variant after incubation with 10% FBS for 48 h analysis by PAGE. ( C ) Flow cytometric assay of HCT116 cells treated with Sgc8 and Sgc8-F23 after incubation with 10% FBS for 0–36 h, illustrating the binding ability after the stability test.
Human Leukemia Cell Ramos, supplied by China Center for Type Culture Collection, 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/result/human leukemia cell ramos/product/China Center for Type Culture Collection
Average 90 stars, based on 1 article reviews
human leukemia cell ramos - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

90
European Collection of Authenticated Cell Cultures ramos cells
In vitro test on the specificity and stability of Sgc8. ( A ) Binding ability <t>to</t> <t>HCT116</t> cells and <t>Ramos</t> cells tested with flow cytometric assay. Unmodified Sgc8 was used as the positive control, and library (lib) was used as the negative control. The cells were incubated with DNAs respectively at a concentration of 250 nM in a binding buffer for 30 min. The incubation temperature was 4°C. ( B ) Stability of Sgc8 variant after incubation with 10% FBS for 48 h analysis by PAGE. ( C ) Flow cytometric assay of HCT116 cells treated with Sgc8 and Sgc8-F23 after incubation with 10% FBS for 0–36 h, illustrating the binding ability after the stability test.
Ramos Cells, supplied by European Collection of Authenticated Cell Cultures, 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/result/ramos cells/product/European Collection of Authenticated Cell Cultures
Average 90 stars, based on 1 article reviews
ramos cells - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


In vitro test on the specificity and stability of Sgc8. ( A ) Binding ability to HCT116 cells and Ramos cells tested with flow cytometric assay. Unmodified Sgc8 was used as the positive control, and library (lib) was used as the negative control. The cells were incubated with DNAs respectively at a concentration of 250 nM in a binding buffer for 30 min. The incubation temperature was 4°C. ( B ) Stability of Sgc8 variant after incubation with 10% FBS for 48 h analysis by PAGE. ( C ) Flow cytometric assay of HCT116 cells treated with Sgc8 and Sgc8-F23 after incubation with 10% FBS for 0–36 h, illustrating the binding ability after the stability test.

Journal: Nucleic Acids Research

Article Title: Programmable manipulation of oligonucleotide–albumin interaction for elongated circulation time

doi: 10.1093/nar/gkac156

Figure Lengend Snippet: In vitro test on the specificity and stability of Sgc8. ( A ) Binding ability to HCT116 cells and Ramos cells tested with flow cytometric assay. Unmodified Sgc8 was used as the positive control, and library (lib) was used as the negative control. The cells were incubated with DNAs respectively at a concentration of 250 nM in a binding buffer for 30 min. The incubation temperature was 4°C. ( B ) Stability of Sgc8 variant after incubation with 10% FBS for 48 h analysis by PAGE. ( C ) Flow cytometric assay of HCT116 cells treated with Sgc8 and Sgc8-F23 after incubation with 10% FBS for 0–36 h, illustrating the binding ability after the stability test.

Article Snippet: Human colon cancer cell line HCT116 was purchased from ATCC, Human leukemia cell Ramos was purchased from China Center for Type Culture Collection (CCTCC, China).

Techniques: In Vitro, Binding Assay, Flow Cytometry, Positive Control, Negative Control, Incubation, Concentration Assay, Variant Assay

The binding affinity of Sgc8 derivatives to albumin. ( A ) Binding affinity analysis of Sgc8 derivatives and Sgc8 with aldehyde/sulfate latex beads coated HSA at room temperature. ( B ) HSA was immobilized to 3.8 μm 40 mg/ml aldehyde/sulfate latex beads (Thermo Fisher Scientific, Waltham, MA USA), after incubation with sgc8 or Sgc8-F23, the beads were washed to remove excess aptamers. The fluorescence signal of HCT116 and Ramos cells treated with the beads (sgc8 or Sgc8-F23 binding with HSA) was collected by flow cytometer.

Journal: Nucleic Acids Research

Article Title: Programmable manipulation of oligonucleotide–albumin interaction for elongated circulation time

doi: 10.1093/nar/gkac156

Figure Lengend Snippet: The binding affinity of Sgc8 derivatives to albumin. ( A ) Binding affinity analysis of Sgc8 derivatives and Sgc8 with aldehyde/sulfate latex beads coated HSA at room temperature. ( B ) HSA was immobilized to 3.8 μm 40 mg/ml aldehyde/sulfate latex beads (Thermo Fisher Scientific, Waltham, MA USA), after incubation with sgc8 or Sgc8-F23, the beads were washed to remove excess aptamers. The fluorescence signal of HCT116 and Ramos cells treated with the beads (sgc8 or Sgc8-F23 binding with HSA) was collected by flow cytometer.

Article Snippet: Human colon cancer cell line HCT116 was purchased from ATCC, Human leukemia cell Ramos was purchased from China Center for Type Culture Collection (CCTCC, China).

Techniques: Binding Assay, Incubation, Fluorescence, Flow Cytometry