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monoclonal anti-hctr1 antibody  (Novus Biologicals)


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    Structured Review

    Novus Biologicals monoclonal anti-hctr1 antibody
    Primer design for the detection of <t> hCTR1 </t> mRNA by RT-LAMP
    Monoclonal Anti Hctr1 Antibody, supplied by Novus Biologicals, 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/monoclonal+anti-hctr1+antibody/rabbit+polyclonal+anti+ctr1+antibody/pmc06958034-48-45-47
    Average 90 stars, based on 1 article reviews
    monoclonal anti-hctr1 antibody - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification"

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification

    Journal: International Journal of Clinical and Experimental Pathology

    doi:

    Primer design for the detection of  hCTR1  mRNA by RT-LAMP
    Figure Legend Snippet: Primer design for the detection of hCTR1 mRNA by RT-LAMP

    Techniques Used: Sequencing

    Sensitivity of LAMP reaction to detect hCTR1. A. The turbidity curve of LAMP technique using a known number of hCTR1 cell copies after 60 min amplification. B. The result of LAMP reaction after 45 min amplification measured by turbidimeter. Lane 1 to 7 was loaded with serially diluted hCTR1 cell copies from one million to one. Lane 8 was loaded as ddH2O as blank control.
    Figure Legend Snippet: Sensitivity of LAMP reaction to detect hCTR1. A. The turbidity curve of LAMP technique using a known number of hCTR1 cell copies after 60 min amplification. B. The result of LAMP reaction after 45 min amplification measured by turbidimeter. Lane 1 to 7 was loaded with serially diluted hCTR1 cell copies from one million to one. Lane 8 was loaded as ddH2O as blank control.

    Techniques Used: Amplification, Control

    Representative hCTR1 over-expressed (A) cervical squamous cell carcinoma and low-expressed carcinoma (B) cases analyzed by immunohistochemical staining and RT-LAMP. In RT-LAMP reaction, carcinoma RNA was loaded into lane 1 to 4 as duplicates, while adjacent normal tissue RNA was loaded into lane 5 to 8 as duplicates. *, P<0.05; **, P>0.05.
    Figure Legend Snippet: Representative hCTR1 over-expressed (A) cervical squamous cell carcinoma and low-expressed carcinoma (B) cases analyzed by immunohistochemical staining and RT-LAMP. In RT-LAMP reaction, carcinoma RNA was loaded into lane 1 to 4 as duplicates, while adjacent normal tissue RNA was loaded into lane 5 to 8 as duplicates. *, P<0.05; **, P>0.05.

    Techniques Used: Immunohistochemical staining, Staining

    Related Articles

    Staining:

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification
    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Immunohistochemistry:

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification
    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Sequencing:

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification
    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Amplification:

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification
    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Control:

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification
    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Immunohistochemical staining:

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification
    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).



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    Image Search Results


    Primer design for the detection of  hCTR1  mRNA by RT-LAMP

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification

    doi:

    Figure Lengend Snippet: Primer design for the detection of hCTR1 mRNA by RT-LAMP

    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Techniques: Sequencing

    Sensitivity of LAMP reaction to detect hCTR1. A. The turbidity curve of LAMP technique using a known number of hCTR1 cell copies after 60 min amplification. B. The result of LAMP reaction after 45 min amplification measured by turbidimeter. Lane 1 to 7 was loaded with serially diluted hCTR1 cell copies from one million to one. Lane 8 was loaded as ddH2O as blank control.

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification

    doi:

    Figure Lengend Snippet: Sensitivity of LAMP reaction to detect hCTR1. A. The turbidity curve of LAMP technique using a known number of hCTR1 cell copies after 60 min amplification. B. The result of LAMP reaction after 45 min amplification measured by turbidimeter. Lane 1 to 7 was loaded with serially diluted hCTR1 cell copies from one million to one. Lane 8 was loaded as ddH2O as blank control.

    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Techniques: Amplification, Control

    Representative hCTR1 over-expressed (A) cervical squamous cell carcinoma and low-expressed carcinoma (B) cases analyzed by immunohistochemical staining and RT-LAMP. In RT-LAMP reaction, carcinoma RNA was loaded into lane 1 to 4 as duplicates, while adjacent normal tissue RNA was loaded into lane 5 to 8 as duplicates. *, P<0.05; **, P>0.05.

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Rapid diagnosis of cisplatin-sensitive and resistant cervical squamous cell carcinomas by reverse transcription loop-mediated isothermal amplification

    doi:

    Figure Lengend Snippet: Representative hCTR1 over-expressed (A) cervical squamous cell carcinoma and low-expressed carcinoma (B) cases analyzed by immunohistochemical staining and RT-LAMP. In RT-LAMP reaction, carcinoma RNA was loaded into lane 1 to 4 as duplicates, while adjacent normal tissue RNA was loaded into lane 5 to 8 as duplicates. *, P<0.05; **, P>0.05.

    Article Snippet: One half was frozen within 30 min after surgery in liquid nitrogen and stored at -80°C until molecular analysis, while the other half was fixed with 10% buffered formalin and embedded in paraffin for routine histopathological examination with H&E staining and IHC examination with monoclonal anti-hCTR1 antibody (Novus, Littleton, USA).

    Techniques: Immunohistochemical staining, Staining