subject atcc cat Search Results


subject atcc cat  (ATCC)
99
ATCC subject atcc cat
Subject Atcc Cat, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ihc for nfatc2  (Proteintech)
93
Proteintech ihc for nfatc2
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Ihc For Nfatc2, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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subject details cell cultures human bone epithelial cell line u2os cells  (ATCC)
99
ATCC subject details cell cultures human bone epithelial cell line u2os cells
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Subject Details Cell Cultures Human Bone Epithelial Cell Line U2os Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mtt assay  (ATCC)
97
ATCC mtt assay
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Mtt Assay, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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murine skeletal muscle cells c2c12  (ATCC)
99
ATCC murine skeletal muscle cells c2c12
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Murine Skeletal Muscle Cells C2c12, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ws1  (ATCC)
96
ATCC ws1
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Ws1, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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experimentalmodeland subject details cell lines human breast cancer cell lines mda mb 231  (ATCC)
99
ATCC experimentalmodeland subject details cell lines human breast cancer cell lines mda mb 231
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Experimentalmodeland Subject Details Cell Lines Human Breast Cancer Cell Lines Mda Mb 231, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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subjects human embryonic kidney 293t cells  (ATCC)
99
ATCC subjects human embryonic kidney 293t cells
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Subjects Human Embryonic Kidney 293t Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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subject details cells n2a cells  (ATCC)
99
ATCC subject details cells n2a cells
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Subject Details Cells N2a Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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subject details cell lines human muscle cell line rd  (ATCC)
99
ATCC subject details cell lines human muscle cell line rd
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Subject Details Cell Lines Human Muscle Cell Line Rd, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human glioblastoma lines u 87 mg  (ATCC)
99
ATCC human glioblastoma lines u 87 mg
Expression of <t>NFATc2</t> in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .
Human Glioblastoma Lines U 87 Mg, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Expression of NFATc2 in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .

Journal: Biomolecules

Article Title: Role of NHERF1 in MicroRNA Landscape Changes in Aging Mouse Kidneys

doi: 10.3390/biom14091048

Figure Lengend Snippet: Expression of NFATc2 in the nuclear fragment of kidneys from WT and NHERF1 −/− mice. Nuclear fractions were prepared from kidney homogenates of 18–24-month-old WT or NHERF1 −/− mice as described in Materials and Methods. Proteins were separated by 10% SDS-PAGE followed by western blotting using an antibody against NFATc2 ( left panel ). A representative blot from kidneys of one male (lanes 1 and 3) and one female (lanes 2 and 4) and the corresponding gel image (stain free image, ( middle panel )) are shown. The bar diagram ( right panel ) shows data as ratio of arbitrary band density to the density of the lane in stain free gel scan (Mean ± SD, n = 3). Data from each individual animal is denoted with a circle on the bar graph. * indicates p < 0.05 from WT kidneys. There were no significant sex differences between the groups, and therefore the data from both males and females were pooled together in the bar diagram. . Original images can be found in .

Article Snippet: Immunohistochemistry: Paraffin-embedded kidney sections were subjected to IHC for NFATc2 (Cat. # 22023-1-AP) and NFATc3 (Cat. # 18222-1-AP) using antibodies from Proteintech (Rosemont, IL, USA) at 1:500 dilution as described previously [ ].

Techniques: Expressing, SDS Page, Western Blot, Staining

Expression of NFATc2 and NFATc3 in kidneys. Representative image of kidneys from 18–24-month-old WT ( left panels ) or NHERF1 −/− ( right panels ) mice ( n = 6, 3 males and 3 females in each group) analyzed by immunohistochemistry for expression of NFATc2 (panel ( B )) and NFATc3 (panel ( C )). Panel ( A ) is a negative control for the antibodies. Arrows show expression staining for NFATc2 ( B ) and NFATc3 ( C ) in the nuclei.

Journal: Biomolecules

Article Title: Role of NHERF1 in MicroRNA Landscape Changes in Aging Mouse Kidneys

doi: 10.3390/biom14091048

Figure Lengend Snippet: Expression of NFATc2 and NFATc3 in kidneys. Representative image of kidneys from 18–24-month-old WT ( left panels ) or NHERF1 −/− ( right panels ) mice ( n = 6, 3 males and 3 females in each group) analyzed by immunohistochemistry for expression of NFATc2 (panel ( B )) and NFATc3 (panel ( C )). Panel ( A ) is a negative control for the antibodies. Arrows show expression staining for NFATc2 ( B ) and NFATc3 ( C ) in the nuclei.

Article Snippet: Immunohistochemistry: Paraffin-embedded kidney sections were subjected to IHC for NFATc2 (Cat. # 22023-1-AP) and NFATc3 (Cat. # 18222-1-AP) using antibodies from Proteintech (Rosemont, IL, USA) at 1:500 dilution as described previously [ ].

Techniques: Expressing, Immunohistochemistry, Negative Control, Staining