hrp labeled sheep anti mouse secondary antibody Search Results


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R&D Systems sheep anti mouse spib polyclonal antibody
Primers used for RT-qPCR analysis.
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Primers used for RT-qPCR analysis.
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R&D Systems sheep anti mouse igg
Primers used for RT-qPCR analysis.
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R&D Systems sheep anti mouse gdf8 propeptide antibody
Primers used for RT-qPCR analysis.
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R&D Systems sheep anti 206 mouse progranulin
Primers used for RT-qPCR analysis.
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Novus Biologicals sheep anti mouse igg horseradish peroxidase conjugate
Primers used for RT-qPCR analysis.
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R&D Systems control sheep igg
Primers used for RT-qPCR analysis.
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Amersham Life Sciences Inc 12i-labeled sheep anti-mouse igg antibodies
Primers used for RT-qPCR analysis.
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Amersham Life Sciences Inc ecl-peroxidase-labeled anti-mouse
Primers used for RT-qPCR analysis.
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Boehringer Mannheim sheep anti-mouse antibody
Primers used for RT-qPCR analysis.
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Becton Dickinson sheep anti-mouse secondary antibody hrp conjugates
Primers used for RT-qPCR analysis.
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NEN Life Science 125 i]-labeled secondary antibody (sheep anti-mouse igg ( 125 i-]f(ab’) 2 fragment
Primers used for RT-qPCR analysis.
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Image Search Results


Primers used for RT-qPCR analysis.

Journal: Immunobiology

Article Title: c-Rel is dispensable for the differentiation and functional maturation of M cells in the follicle-associated epithelium

doi: 10.1016/j.imbio.2016.09.008

Figure Lengend Snippet: Primers used for RT-qPCR analysis.

Article Snippet: For the detection of SpiB in paraformaldehyde-fixed sections, antigen retrieval was performed with citrate buffer (pH 7.0, 121 °C, 5 min) prior to immunostaining with sheep anti-mouse SpiB polyclonal antibody (R&D Systems).

Techniques:

SpiB expression in the FAE is unaffected in the absence of c-Rel. (A) IHC analysis of SpiB expression (green) in the FAE of c-Rel −/− and wild-type (WT) control mice. Boxed areas in upper panels are shown at higher magnification in the lower panels. Broken lines indicate the FAE boundaries. Arrows, Spi-B + cell nuclei in the FAE. (B) Morphometric analysis showed that the number of SpiB + cells in the FAE of c-Rel −/− and WT were similar. (C) RT-qPCR analysis suggested there was no significant difference in the expression of Spib mRNA levels in Peyer’s patches from c-Rel −/− or WT mice. Gene expression data are normalised so that the mean level in samples from WT mice was 1.0. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Journal: Immunobiology

Article Title: c-Rel is dispensable for the differentiation and functional maturation of M cells in the follicle-associated epithelium

doi: 10.1016/j.imbio.2016.09.008

Figure Lengend Snippet: SpiB expression in the FAE is unaffected in the absence of c-Rel. (A) IHC analysis of SpiB expression (green) in the FAE of c-Rel −/− and wild-type (WT) control mice. Boxed areas in upper panels are shown at higher magnification in the lower panels. Broken lines indicate the FAE boundaries. Arrows, Spi-B + cell nuclei in the FAE. (B) Morphometric analysis showed that the number of SpiB + cells in the FAE of c-Rel −/− and WT were similar. (C) RT-qPCR analysis suggested there was no significant difference in the expression of Spib mRNA levels in Peyer’s patches from c-Rel −/− or WT mice. Gene expression data are normalised so that the mean level in samples from WT mice was 1.0. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Article Snippet: For the detection of SpiB in paraformaldehyde-fixed sections, antigen retrieval was performed with citrate buffer (pH 7.0, 121 °C, 5 min) prior to immunostaining with sheep anti-mouse SpiB polyclonal antibody (R&D Systems).

Techniques: Expressing, Control, Quantitative RT-PCR, Gene Expression