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anti tetanus mcab mca2849  (Bio-Rad)


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    Structured Review

    Bio-Rad anti tetanus mcab mca2849
    The cell suspensions (2×10 4 cells) mixed with 0.3% agarose and different concentrations of NJ001 or <t>MCA2849</t> were layered on the top of culture media in 6-well culture plates and allowed to grow for 2 weeks before colonies were counted. Representative contrast images were shown. (A) 0 µg/mL NJ001, (B) 100 µg/mL NJ001, (C) 200 µg/mL NJ001, (D) 400 µg/mL NJ001, (E) 0 µg/mL MCA2849, (F) 100 µg/mL MCA2849, (G) 200 µg/mL MCA2849, (H) 400 µg/mL MCA2849.
    Anti Tetanus Mcab Mca2849, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+tetanus+mcab+mca2849/Mouse+anti+Clostridium+tetani+Tetanus+Toxin/pmc03316548-159-0-3
    Average 93 stars, based on 1 article reviews
    anti tetanus mcab mca2849 - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics"

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0033009

    The cell suspensions (2×10 4 cells) mixed with 0.3% agarose and different concentrations of NJ001 or MCA2849 were layered on the top of culture media in 6-well culture plates and allowed to grow for 2 weeks before colonies were counted. Representative contrast images were shown. (A) 0 µg/mL NJ001, (B) 100 µg/mL NJ001, (C) 200 µg/mL NJ001, (D) 400 µg/mL NJ001, (E) 0 µg/mL MCA2849, (F) 100 µg/mL MCA2849, (G) 200 µg/mL MCA2849, (H) 400 µg/mL MCA2849.
    Figure Legend Snippet: The cell suspensions (2×10 4 cells) mixed with 0.3% agarose and different concentrations of NJ001 or MCA2849 were layered on the top of culture media in 6-well culture plates and allowed to grow for 2 weeks before colonies were counted. Representative contrast images were shown. (A) 0 µg/mL NJ001, (B) 100 µg/mL NJ001, (C) 200 µg/mL NJ001, (D) 400 µg/mL NJ001, (E) 0 µg/mL MCA2849, (F) 100 µg/mL MCA2849, (G) 200 µg/mL MCA2849, (H) 400 µg/mL MCA2849.

    Techniques Used:

    <xref ref-type= Results of colony formation of SPC-A1 cells treated by NJ001 or MCA2849 in soft agar." title="... formation of SPC-A1 cells treated by NJ001 or MCA2849 in soft agar." property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: Results of colony formation of SPC-A1 cells treated by NJ001 or MCA2849 in soft agar.

    Techniques Used:

    SPC-A1 cells were cultured with or without 200 µg/mL NJ001 or MCA2849 for 24 h and 48 h. (A) Morphological changes in SPC-A1 cells were observed under inverted microscope (×100). a, 24 h NJ001; b, 24 h MCA2849; c, 24 h McAb free; d, 48 h NJ001; e, 48 h MCA2849; f, 48 h McAb free. (B) Apoptosis was analyzed by flow cytometry. (C) Each column and error bar represents the mean ± SD of three independent experiments (** P <0.001). The amount of late apoptosis was determined as the percentage of Annexin V + /PI + cells.
    Figure Legend Snippet: SPC-A1 cells were cultured with or without 200 µg/mL NJ001 or MCA2849 for 24 h and 48 h. (A) Morphological changes in SPC-A1 cells were observed under inverted microscope (×100). a, 24 h NJ001; b, 24 h MCA2849; c, 24 h McAb free; d, 48 h NJ001; e, 48 h MCA2849; f, 48 h McAb free. (B) Apoptosis was analyzed by flow cytometry. (C) Each column and error bar represents the mean ± SD of three independent experiments (** P <0.001). The amount of late apoptosis was determined as the percentage of Annexin V + /PI + cells.

    Techniques Used: Cell Culture, Inverted Microscopy, Flow Cytometry

    Related Articles

    Cell Culture:

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics
    Article Snippet: This experiment was repeated 3 times.This experiment was repeated 3 times.. Anti-tetanus McAb (MCA2849) (AbD Serotec, Germany) was used as irrelevant McAb in this study.

    Inverted Microscopy:

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics
    Article Snippet: This experiment was repeated 3 times.This experiment was repeated 3 times.. Anti-tetanus McAb (MCA2849) (AbD Serotec, Germany) was used as irrelevant McAb in this study.

    Flow Cytometry:

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics
    Article Snippet: This experiment was repeated 3 times.This experiment was repeated 3 times.. Anti-tetanus McAb (MCA2849) (AbD Serotec, Germany) was used as irrelevant McAb in this study.



    Similar Products

    93
    Bio-Rad anti tetanus mcab mca2849
    The cell suspensions (2×10 4 cells) mixed with 0.3% agarose and different concentrations of NJ001 or <t>MCA2849</t> were layered on the top of culture media in 6-well culture plates and allowed to grow for 2 weeks before colonies were counted. Representative contrast images were shown. (A) 0 µg/mL NJ001, (B) 100 µg/mL NJ001, (C) 200 µg/mL NJ001, (D) 400 µg/mL NJ001, (E) 0 µg/mL MCA2849, (F) 100 µg/mL MCA2849, (G) 200 µg/mL MCA2849, (H) 400 µg/mL MCA2849.
    Anti Tetanus Mcab Mca2849, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+tetanus+mcab+mca2849/Mouse+anti+Clostridium+tetani+Tetanus+Toxin/pmc03316548-159-0-3
    Average 93 stars, based on 1 article reviews
    anti tetanus mcab mca2849 - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    Image Search Results


    The cell suspensions (2×10 4 cells) mixed with 0.3% agarose and different concentrations of NJ001 or MCA2849 were layered on the top of culture media in 6-well culture plates and allowed to grow for 2 weeks before colonies were counted. Representative contrast images were shown. (A) 0 µg/mL NJ001, (B) 100 µg/mL NJ001, (C) 200 µg/mL NJ001, (D) 400 µg/mL NJ001, (E) 0 µg/mL MCA2849, (F) 100 µg/mL MCA2849, (G) 200 µg/mL MCA2849, (H) 400 µg/mL MCA2849.

    Journal: PLoS ONE

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics

    doi: 10.1371/journal.pone.0033009

    Figure Lengend Snippet: The cell suspensions (2×10 4 cells) mixed with 0.3% agarose and different concentrations of NJ001 or MCA2849 were layered on the top of culture media in 6-well culture plates and allowed to grow for 2 weeks before colonies were counted. Representative contrast images were shown. (A) 0 µg/mL NJ001, (B) 100 µg/mL NJ001, (C) 200 µg/mL NJ001, (D) 400 µg/mL NJ001, (E) 0 µg/mL MCA2849, (F) 100 µg/mL MCA2849, (G) 200 µg/mL MCA2849, (H) 400 µg/mL MCA2849.

    Article Snippet: Anti-tetanus McAb (MCA2849) (AbD Serotec, Germany) was used as irrelevant McAb in this study.

    Techniques:

    <xref ref-type= Results of colony formation of SPC-A1 cells treated by NJ001 or MCA2849 in soft agar." width="100%" height="100%">

    Journal: PLoS ONE

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics

    doi: 10.1371/journal.pone.0033009

    Figure Lengend Snippet: Results of colony formation of SPC-A1 cells treated by NJ001 or MCA2849 in soft agar.

    Article Snippet: Anti-tetanus McAb (MCA2849) (AbD Serotec, Germany) was used as irrelevant McAb in this study.

    Techniques:

    SPC-A1 cells were cultured with or without 200 µg/mL NJ001 or MCA2849 for 24 h and 48 h. (A) Morphological changes in SPC-A1 cells were observed under inverted microscope (×100). a, 24 h NJ001; b, 24 h MCA2849; c, 24 h McAb free; d, 48 h NJ001; e, 48 h MCA2849; f, 48 h McAb free. (B) Apoptosis was analyzed by flow cytometry. (C) Each column and error bar represents the mean ± SD of three independent experiments (** P <0.001). The amount of late apoptosis was determined as the percentage of Annexin V + /PI + cells.

    Journal: PLoS ONE

    Article Title: The Study on Newly Developed McAb NJ001 Specific to Non-Small Cell Lung Cancer and Its Biological Characteristics

    doi: 10.1371/journal.pone.0033009

    Figure Lengend Snippet: SPC-A1 cells were cultured with or without 200 µg/mL NJ001 or MCA2849 for 24 h and 48 h. (A) Morphological changes in SPC-A1 cells were observed under inverted microscope (×100). a, 24 h NJ001; b, 24 h MCA2849; c, 24 h McAb free; d, 48 h NJ001; e, 48 h MCA2849; f, 48 h McAb free. (B) Apoptosis was analyzed by flow cytometry. (C) Each column and error bar represents the mean ± SD of three independent experiments (** P <0.001). The amount of late apoptosis was determined as the percentage of Annexin V + /PI + cells.

    Article Snippet: Anti-tetanus McAb (MCA2849) (AbD Serotec, Germany) was used as irrelevant McAb in this study.

    Techniques: Cell Culture, Inverted Microscopy, Flow Cytometry