mda mb 435  (ATCC)


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    ATCC mda mb 435
    Mda Mb 435, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mda mb 435s  (ATCC)


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    ATCC mda mb 435s
    Mda Mb 435s, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    human mda mb 435s  (ATCC)


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    ATCC human mda mb 435s
    Human Mda Mb 435s, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mda mb 435  (ATCC)


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    ATCC mda mb 435
    CTCF and BORIS co-binding to intronic regions of GAL3ST1 and FER genes associated with cancer-testis-specific transcription. a,b Above: Schematic representation of the gene structure of GAL3ST1 ( a ) and FER ( b ). Arrows denote somatic (black) and testis-specific (red) TSSs. Below: In the upper part, ChIP-seq peaks illustrate CTCF (red) and BORIS (blue) co-binding in BORIS-positive (BORIS +) K562 cells across GAL3ST1 and FER (exon 7-10). The co-binding coincides with the enrichment of active histones/marks H3K4me3 (purple), H2A.Z (magenta), and RNAPII (brown). RNA-seq peaks (indigo) and CAGE-seq peaks (pink) highlight alternative transcription in K562 cells. In the lower part, CTCF binding alone in BORIS-negative (BORIS −) NHEK cells does not activate testis-specific promoters. CAGE-seq for human testes (pink) is shown between the two panels, with red boxes highlighting testis-specific TSSs. c–e In the upper part, Western blots from whole cell lysates show BORIS protein detection in c K562 wild-type (WT1-total culture, WT2 and WT3 – single-cell wild-type clones transfected with control RNA) versus BORIS knockdown (kd) K562 single-cell clones (#3,4,7), obtained by zinc finger nuclease (ZFN) treatment. d HEK293T and e <t>MDA-MB-435</t> cells transfected with empty (EV) or BORIS-expressing vector. Tubulin is used as a loading control. Numbers (1,2,3) indicate different single-cell clones. The middle part displays RT-qPCR results indicating the relative expression of GAL3ST1 and FERT in K562, HEK293T, and MDA-MB-435 cell lines. Statistical analysis was performed using two-tailed Student’s t test (*, p < 0.0005). Error bars indicate mean ± SD ( n = 3), ns – non-significant. In the bottom part, ChIP-seq peaks show CTCF and BORIS occupancy in K562 (clone#7) BORIS kd cells, HEK293T, and MDA-MB-435 cells. Abbreviations; Ref. TSS (reference transcriptional start site), Alt. TSS (alternative transcriptional start site)
    Mda Mb 435, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "BORIS/CTCFL epigenetically reprograms clustered CTCF binding sites into alternative transcriptional start sites"

    Article Title: BORIS/CTCFL epigenetically reprograms clustered CTCF binding sites into alternative transcriptional start sites

    Journal: Genome Biology

    doi: 10.1186/s13059-024-03175-0

    CTCF and BORIS co-binding to intronic regions of GAL3ST1 and FER genes associated with cancer-testis-specific transcription. a,b Above: Schematic representation of the gene structure of GAL3ST1 ( a ) and FER ( b ). Arrows denote somatic (black) and testis-specific (red) TSSs. Below: In the upper part, ChIP-seq peaks illustrate CTCF (red) and BORIS (blue) co-binding in BORIS-positive (BORIS +) K562 cells across GAL3ST1 and FER (exon 7-10). The co-binding coincides with the enrichment of active histones/marks H3K4me3 (purple), H2A.Z (magenta), and RNAPII (brown). RNA-seq peaks (indigo) and CAGE-seq peaks (pink) highlight alternative transcription in K562 cells. In the lower part, CTCF binding alone in BORIS-negative (BORIS −) NHEK cells does not activate testis-specific promoters. CAGE-seq for human testes (pink) is shown between the two panels, with red boxes highlighting testis-specific TSSs. c–e In the upper part, Western blots from whole cell lysates show BORIS protein detection in c K562 wild-type (WT1-total culture, WT2 and WT3 – single-cell wild-type clones transfected with control RNA) versus BORIS knockdown (kd) K562 single-cell clones (#3,4,7), obtained by zinc finger nuclease (ZFN) treatment. d HEK293T and e MDA-MB-435 cells transfected with empty (EV) or BORIS-expressing vector. Tubulin is used as a loading control. Numbers (1,2,3) indicate different single-cell clones. The middle part displays RT-qPCR results indicating the relative expression of GAL3ST1 and FERT in K562, HEK293T, and MDA-MB-435 cell lines. Statistical analysis was performed using two-tailed Student’s t test (*, p < 0.0005). Error bars indicate mean ± SD ( n = 3), ns – non-significant. In the bottom part, ChIP-seq peaks show CTCF and BORIS occupancy in K562 (clone#7) BORIS kd cells, HEK293T, and MDA-MB-435 cells. Abbreviations; Ref. TSS (reference transcriptional start site), Alt. TSS (alternative transcriptional start site)
    Figure Legend Snippet: CTCF and BORIS co-binding to intronic regions of GAL3ST1 and FER genes associated with cancer-testis-specific transcription. a,b Above: Schematic representation of the gene structure of GAL3ST1 ( a ) and FER ( b ). Arrows denote somatic (black) and testis-specific (red) TSSs. Below: In the upper part, ChIP-seq peaks illustrate CTCF (red) and BORIS (blue) co-binding in BORIS-positive (BORIS +) K562 cells across GAL3ST1 and FER (exon 7-10). The co-binding coincides with the enrichment of active histones/marks H3K4me3 (purple), H2A.Z (magenta), and RNAPII (brown). RNA-seq peaks (indigo) and CAGE-seq peaks (pink) highlight alternative transcription in K562 cells. In the lower part, CTCF binding alone in BORIS-negative (BORIS −) NHEK cells does not activate testis-specific promoters. CAGE-seq for human testes (pink) is shown between the two panels, with red boxes highlighting testis-specific TSSs. c–e In the upper part, Western blots from whole cell lysates show BORIS protein detection in c K562 wild-type (WT1-total culture, WT2 and WT3 – single-cell wild-type clones transfected with control RNA) versus BORIS knockdown (kd) K562 single-cell clones (#3,4,7), obtained by zinc finger nuclease (ZFN) treatment. d HEK293T and e MDA-MB-435 cells transfected with empty (EV) or BORIS-expressing vector. Tubulin is used as a loading control. Numbers (1,2,3) indicate different single-cell clones. The middle part displays RT-qPCR results indicating the relative expression of GAL3ST1 and FERT in K562, HEK293T, and MDA-MB-435 cell lines. Statistical analysis was performed using two-tailed Student’s t test (*, p < 0.0005). Error bars indicate mean ± SD ( n = 3), ns – non-significant. In the bottom part, ChIP-seq peaks show CTCF and BORIS occupancy in K562 (clone#7) BORIS kd cells, HEK293T, and MDA-MB-435 cells. Abbreviations; Ref. TSS (reference transcriptional start site), Alt. TSS (alternative transcriptional start site)

    Techniques Used: Binding Assay, ChIP-sequencing, RNA Sequencing Assay, Western Blot, Clone Assay, Transfection, Zinc-Fingers, Expressing, Plasmid Preparation, Quantitative RT-PCR, Two Tailed Test

    cell line mda mb 435s  (ATCC)


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    ATCC cell line mda mb 435s
    Cell Line Mda Mb 435s, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mda mb 435 cells  (ATCC)


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    ATCC mda mb 435 cells
    Total cellular protein from <t>MDA-MB-435</t> cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.
    Mda Mb 435 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Cellular distribution and motion of essential magnetosome proteins expressed in mammalian cells"

    Article Title: Cellular distribution and motion of essential magnetosome proteins expressed in mammalian cells

    Journal: bioRxiv

    doi: 10.1101/2023.12.19.572414

    Total cellular protein from MDA-MB-435 cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.

    Techniques Used: Stable Transfection, Expressing, Western Blot

    Total cellular protein from MDA-MB-435 cells stably expressing EGFP-MamE was examined with mouse α-EGFP. The full-length western blot is displayed.
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing EGFP-MamE was examined with mouse α-EGFP. The full-length western blot is displayed.

    Techniques Used: Stable Transfection, Expressing, Western Blot

    Total cellular protein content from MDA-MB-435 cells stably expressing Tomato or Tomato-MamB were examined by western blot using rabbit α-Tomato as the primary antibody. The approximate size of Tomato-MamB is 91 kDa (red arrow). Approximate MW is shown in the left margin.
    Figure Legend Snippet: Total cellular protein content from MDA-MB-435 cells stably expressing Tomato or Tomato-MamB were examined by western blot using rabbit α-Tomato as the primary antibody. The approximate size of Tomato-MamB is 91 kDa (red arrow). Approximate MW is shown in the left margin.

    Techniques Used: Stable Transfection, Expressing, Western Blot

    Total cellular protein from MDA-MB-435 cells stably expressing Tomato-MamB was examined with rabbit α-Tomato. The full-length western blot is displayed.
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing Tomato-MamB was examined with rabbit α-Tomato. The full-length western blot is displayed.

    Techniques Used: Stable Transfection, Expressing, Western Blot

    mda mb 435 cells  (ATCC)


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    ATCC mda mb 435 cells
    Total cellular protein from <t>MDA-MB-435</t> cells stably expressing either EGFP or EGFP-MamI ( A ), Tomato or Tomato-MamL ( B ), or both magnetosome fusion proteins ( C ) was examined by western blot, using mouse α-EGFP ( A , C ) and/or rabbit α-Tomato ( B , C ) as the primary antibodies. Type of fluorescent protein expressed by the cells is indicated above each lane. In panel C, the same cell sample was probed for each magnetosome fusion protein. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panels). Full-length blots are presented in .
    Mda Mb 435 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Essential magnetosome proteins MamI and MamL from magnetotactic bacteria interact in mammalian cells"

    Article Title: Essential magnetosome proteins MamI and MamL from magnetotactic bacteria interact in mammalian cells

    Journal: bioRxiv

    doi: 10.1101/2023.12.19.572379

    Total cellular protein from MDA-MB-435 cells stably expressing either EGFP or EGFP-MamI ( A ), Tomato or Tomato-MamL ( B ), or both magnetosome fusion proteins ( C ) was examined by western blot, using mouse α-EGFP ( A , C ) and/or rabbit α-Tomato ( B , C ) as the primary antibodies. Type of fluorescent protein expressed by the cells is indicated above each lane. In panel C, the same cell sample was probed for each magnetosome fusion protein. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panels). Full-length blots are presented in .
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing either EGFP or EGFP-MamI ( A ), Tomato or Tomato-MamL ( B ), or both magnetosome fusion proteins ( C ) was examined by western blot, using mouse α-EGFP ( A , C ) and/or rabbit α-Tomato ( B , C ) as the primary antibodies. Type of fluorescent protein expressed by the cells is indicated above each lane. In panel C, the same cell sample was probed for each magnetosome fusion protein. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panels). Full-length blots are presented in .

    Techniques Used: Stable Transfection, Expressing, Western Blot

    Total cellular protein from MDA-MB-435 cells stably expressing either Tomato, Tomato-MamL, Tomato-MamL trunc , or both EGFP-MamI and Tomato-MamL trunc was examined by western blot. Type of fluorescent protein expressed by the cells is indicated above each lane. For EGFP-MamI/Tomato-MamL trunc extracts, the same cell sample was probed for each magnetosome fusion protein. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panel). Full-length blots are presented in .
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing either Tomato, Tomato-MamL, Tomato-MamL trunc , or both EGFP-MamI and Tomato-MamL trunc was examined by western blot. Type of fluorescent protein expressed by the cells is indicated above each lane. For EGFP-MamI/Tomato-MamL trunc extracts, the same cell sample was probed for each magnetosome fusion protein. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panel). Full-length blots are presented in .

    Techniques Used: Stable Transfection, Expressing, Western Blot

    Micrographs display a population of MDA-MB-435 cells co-expressing FLAG-tagged MamL and EGFP-MamI fusion protein. The punctate intracellular fluorescence revealed by EGFP-MamI is similar to that obtained with two fluorescent fusion proteins (Tomato-MamL and EGFP-MamI, ). Mobile punctate structures are dispersed throughout the cell (Movie 6).
    Figure Legend Snippet: Micrographs display a population of MDA-MB-435 cells co-expressing FLAG-tagged MamL and EGFP-MamI fusion protein. The punctate intracellular fluorescence revealed by EGFP-MamI is similar to that obtained with two fluorescent fusion proteins (Tomato-MamL and EGFP-MamI, ). Mobile punctate structures are dispersed throughout the cell (Movie 6).

    Techniques Used: Expressing, Fluorescence

    Total cellular protein from MDA-MB-435 cells stably expressing both FLAG-MamL and EGFP-MamI was examined by western blot using primary α-FLAG and α-EGFP antibodies. The same sample was probed in both lanes. Approximate size of FLAG-MamL is 11 kDa. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panels). Full-length blots are presented in .
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing both FLAG-MamL and EGFP-MamI was examined by western blot using primary α-FLAG and α-EGFP antibodies. The same sample was probed in both lanes. Approximate size of FLAG-MamL is 11 kDa. Approximate MW is shown in the left margin. The loading control was GAPDH (bottom panels). Full-length blots are presented in .

    Techniques Used: Stable Transfection, Expressing, Western Blot

    Total cellular protein from MDA-MB-435 cells stably expressing Tomato, Tomato-MamL, Tomato-MamL trunc , and co-expressing Tomato-MamL trunc /EGFP-MamI were examined with rabbit α-Tomato or mouse α-EGFP (far right lane). Full-length western blots are displayed.
    Figure Legend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing Tomato, Tomato-MamL, Tomato-MamL trunc , and co-expressing Tomato-MamL trunc /EGFP-MamI were examined with rabbit α-Tomato or mouse α-EGFP (far right lane). Full-length western blots are displayed.

    Techniques Used: Stable Transfection, Expressing, Western Blot

    mda mb 435s  (ATCC)


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    ATCC mda mb 435s
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    mda mb 435s human breast cancer line  (ATCC)


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    ATCC mda mb 435s human breast cancer line
    Mda Mb 435s Human Breast Cancer Line, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mda mb 435  (ATCC)


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    ATCC mda mb 435
    Mda Mb 435, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC mda mb 435
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    ATCC mda mb 435s
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    ATCC human mda mb 435s
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    ATCC cell line mda mb 435s
    Cell Line Mda Mb 435s, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC mda mb 435 cells
    Total cellular protein from <t>MDA-MB-435</t> cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.
    Mda Mb 435 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC mda mb 435s human breast cancer line
    Total cellular protein from <t>MDA-MB-435</t> cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.
    Mda Mb 435s Human Breast Cancer Line, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mda mb 435s human breast cancer line/product/ATCC
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    Total cellular protein from MDA-MB-435 cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.

    Journal: bioRxiv

    Article Title: Cellular distribution and motion of essential magnetosome proteins expressed in mammalian cells

    doi: 10.1101/2023.12.19.572414

    Figure Lengend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing EGFP or EGFP-MamE (G49S, T641S) were examined by western blot using mouse α-EGFP as the primary antibody. The approximate size of EGFP-MamE is 110 kDa (red arrow). Bands at lower molecular weights are products of MamE proteolysis . Approximate MW is shown in the left margin. The loading control was GAPDH and appears in the bottom panels.

    Article Snippet: MDA-MB-435 cells (ATCC HTB-129; derived from an adult female and characterized as a melanoma cell line) are a model of aggressive tumorigenesis ( ).

    Techniques: Stable Transfection, Expressing, Western Blot

    Total cellular protein from MDA-MB-435 cells stably expressing EGFP-MamE was examined with mouse α-EGFP. The full-length western blot is displayed.

    Journal: bioRxiv

    Article Title: Cellular distribution and motion of essential magnetosome proteins expressed in mammalian cells

    doi: 10.1101/2023.12.19.572414

    Figure Lengend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing EGFP-MamE was examined with mouse α-EGFP. The full-length western blot is displayed.

    Article Snippet: MDA-MB-435 cells (ATCC HTB-129; derived from an adult female and characterized as a melanoma cell line) are a model of aggressive tumorigenesis ( ).

    Techniques: Stable Transfection, Expressing, Western Blot

    Total cellular protein content from MDA-MB-435 cells stably expressing Tomato or Tomato-MamB were examined by western blot using rabbit α-Tomato as the primary antibody. The approximate size of Tomato-MamB is 91 kDa (red arrow). Approximate MW is shown in the left margin.

    Journal: bioRxiv

    Article Title: Cellular distribution and motion of essential magnetosome proteins expressed in mammalian cells

    doi: 10.1101/2023.12.19.572414

    Figure Lengend Snippet: Total cellular protein content from MDA-MB-435 cells stably expressing Tomato or Tomato-MamB were examined by western blot using rabbit α-Tomato as the primary antibody. The approximate size of Tomato-MamB is 91 kDa (red arrow). Approximate MW is shown in the left margin.

    Article Snippet: MDA-MB-435 cells (ATCC HTB-129; derived from an adult female and characterized as a melanoma cell line) are a model of aggressive tumorigenesis ( ).

    Techniques: Stable Transfection, Expressing, Western Blot

    Total cellular protein from MDA-MB-435 cells stably expressing Tomato-MamB was examined with rabbit α-Tomato. The full-length western blot is displayed.

    Journal: bioRxiv

    Article Title: Cellular distribution and motion of essential magnetosome proteins expressed in mammalian cells

    doi: 10.1101/2023.12.19.572414

    Figure Lengend Snippet: Total cellular protein from MDA-MB-435 cells stably expressing Tomato-MamB was examined with rabbit α-Tomato. The full-length western blot is displayed.

    Article Snippet: MDA-MB-435 cells (ATCC HTB-129; derived from an adult female and characterized as a melanoma cell line) are a model of aggressive tumorigenesis ( ).

    Techniques: Stable Transfection, Expressing, Western Blot