fluorchem 8800 Search Results


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Fluorchem 8800 Station, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Alpha Innotech densitometry fluorchem 8800
Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by <t>densitometry</t> using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.
Densitometry Fluorchem 8800, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Alpha Innotech fluorchem 8800 ccd imaging system equipped with automatic bloom detection
Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by <t>densitometry</t> using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.
Fluorchem 8800 Ccd Imaging System Equipped With Automatic Bloom Detection, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by <t>densitometry</t> using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.
Alphaeasefc Fluorchem 8800, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by <t>densitometry</t> using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.
Alphaease Fc Fluorchem 8800 Software, Version 3.1.2, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Alpha Innotech fluorchem 8800 detector
Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by <t>densitometry</t> using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.
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Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by <t>densitometry</t> using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.
Alphaeascfc Fluorchem 8800 Imaging System, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by densitometry using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.

Journal: Biology of Reproduction

Article Title: Plasma Membrane Ca 2+ -ATPase 4 in Murine Epididymis: Secretion of Splice Variants in the Luminal Fluid and a Role in Sperm Maturation 1

doi: 10.1095/biolreprod.113.108712

Figure Lengend Snippet: Western blot analysis of PMCA4a expression in murine testis and epididymal tissue (A) and ELF (B, D). Twenty and 45 μg of protein/lane were loaded in A and B, respectively. PMCA4a was detected using a rabbit polyclonal anti-bovine PMCA4a antibody (1:175 dilution) in A, and a rabbit polyclonal anti-rat PMCA4a antibody (1:500 dilution) in B. A shows the presence of PMCA4a in the testis and all three epididymal regions, while B shows PMCA4a in purified ELF from each of the three epididymal regions. Blots of the latter were stripped and reprobed for β-actin as a loading control, and PMCA4a band intensities were analyzed by densitometry using Image J software. The relative expression in corpus/cauda compared to the caput is displayed in a bar graph in C. Values are expressed as means ± SD (n = 3), with expression highest in the cauda (*P = 0.014 versus caput). D shows immunoblotting of proteins from pellet and supernatant fractions of equivalent volumes of ELF, following ultracentrifugation. PMCA4a, seen in the pellet, is absent from the supernatant. An immunopositive band (100 kDa) which is also seen in A is of unknown origin, but most likely a breakdown product as it is much fainter in the unprocessed ELF and is not seen in B.

Article Snippet: Protein bands were analyzed by densitometry (FluorChem 8800; Alpha Innotech Corp.), and the ratio of PMCA4a to the loading controls was determined and plotted.

Techniques: Western Blot, Expressing, Purification, Control, Software