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Rat anti cd8

Manufactured by Abcam
Sourced in United States

Rat anti-CD8 is an antibody that binds to the CD8 protein found on the surface of certain T cells. CD8 is a co-receptor that assists in the activation of cytotoxic T cells. The antibody can be used for the identification and analysis of CD8-positive T cells in research applications.

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2 protocols using rat anti cd8

1

Immunohistochemical Analysis of EPRAP and Associated Pathways

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Rabbit polyclonal antibody against mouse EPRAP was raised by immunization with keyhole limpet hemocyanin–conjugated synthetic peptides corresponding to amino-acid residues 244–260, 330–346, and 629–645 of murine EPRAP. For immunohistochemistry of mouse samples, paraffin-embedded sections were routinely stained with one of the following antibodies: rat anti-F4/80 (Abcam, Cambridge, MA, USA), rat anti–Gr-1 (eBioscience, San Diego, CA, USA), rat anti-B220 (eBioscience), rat anti-CD4 (eBioscience), rat anti-CD8 (Abcam), hamster anti-CD11c (eBioscience), mouse anti-NCAM (Abcam), rabbit anti–phospho-NF-κB p105 (Ser933) (Cell Signaling, Boston, MA, USA), rabbit anti–phospho-MEK1/2 (Ser221) (Cell Signaling), or rabbit anti–phospho-p44/42 MAPK (Thr202/Tyr204) (Cell Signaling), or rabbit anti-EPRAP.
For immunohistochemistry of human samples, paraffin-embedded sections were stained with rat anti-CD68 (Abcam), goat anti-FEM1A (Abcam), and rabbit anti–phospho-NF-κB p105 (Ser933), rabbit anti–phospho-MEK1/2 (Ser221), or rabbit anti–phospho-p44/42 MAPK (Thr202/Tyr204) antibodies. Staining with non-immune rat or rabbit IgG served as a negative control for each experiment.
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2

Immunostaining of Thymic Tissue

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Unfixed thymi were embedded in OCT compound (Sakura, Chuo-ku, Tokyo, Japan), cut, fixed in acetone and stained as previously described.49 (link) The primary Abs used were rabbit anti-FADD (EP887Y), rabbit anti-Notch1 (EP1238Y), rabbit anti-Jagged1 (EPR4290), rabbit anti-Jagged2 (EPR3646) (Epitomics), rabbit anti-NKAP (Sigma), rat anti-CD4 (GK1.5), rat anti-CD8 (YTS169.4), rabbit anti-DL1 (30B11.1(14)), rabbit anti-DL4 (Abcam, Cambridge, MA, USA), rat anti-CD44 (IM7), and biotinylated rat anti-CD25(PC61) (BD Biosciences). Secondary reagents used were Alexa 488-streptavidin, Alexa 488 and Alexa 594-conjugated goat anti-rabbit IgG (Jackson ImmunoResearch, West Grove, PA, USA). Sections were first blocked for 1 h using 4% goat serum, then labeled with primary Abs followed by the secondary Abs. Nuclear DNA was stained using 4′, 6-diamidino-2-phenylindole (DAPI). Images were then visualized by microscopy (Carl Zeiss Axioplan 2, Göttingen, Germany).
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