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Irdye 800cw goat anti rabbit igg h l antibody

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The IRDye 800CW goat anti-rabbit IgG (H+L) antibody is a fluorescently-labeled secondary antibody designed for use in near-infrared (NIR) fluorescence-based detection and imaging applications. The antibody targets the heavy and light chains of rabbit immunoglobulin G (IgG) and is conjugated with the IRDye 800CW fluorescent dye, which has an excitation/emission spectrum suitable for NIR detection.

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IRDye 800CW goat anti-rabbit IgG (308 citations) IRDye 800CW goat anti-rabbit (264 citations) IRDye 800CW goat anti-rabbit IgG (H+L) (75 citations) IRDye 800CW anti-rabbit IgG (35 citations) IRDye 800CW goat anti-rabbit antibody (30 citations) 800CW goat anti-rabbit IgG (8 citations) Goat anti-rabbit IgG (H+L) (4 citations) IRDye 800CW anti-rabbit IgG (H+L) (3 citations) IRDye® 800CW goat anti-rabbit IgG antibody (2 citations) IRDye 800CW anti-rabbit antibody (2 citations)

2 protocols using irdye 800cw goat anti rabbit igg h l antibody

1

PCNA Protein Expression Quantification

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The other half of each tumor was snap-frozen in liquid nitrogen. Then, the total protein was extracted. PCNA was detected by normal Western blotting with the same anti-PCNA antibody as that used in the immunohistochemistry experiment. IRDye 800CW goat anti-rabbit IgG (H+L) antibody (LI-COR Biosciences, Lincoln, NE, USA) was used as the secondary antibody. β-actin was also detected as an internal control. Images were obtained by Odyssey (LI-COR, USA) and intensity quantifications of the Western blot bands were performed by ImageJ software (National Institutes of Health, USA).
Zhang Q., Zhang Y., Li K., Wang H., Li H, & Zheng J. (2015). A Novel Strategy to Improve the Therapeutic Efficacy of Gemcitabine for Non-Small Cell Lung Cancer by the Tumor-Penetrating Peptide iRGD. PLoS ONE, 10(6), e0129865.
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2

Peptide-Induced MAPK Phosphorylation in Rice

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Proteins were extracted from rice leaves and panicles after treatment with synthesized peptides using a plant phosphorylated protein extraction kit (HR0011, Baiaolaibo) following the manufacturer’s instructions. Phosphorylation of MAPK proteins was detected by immunoblotting with anti‐pMAPK antibody (#4370 s, Cell Signaling, 1:1000) and IRDye 800CW Goat anti-Rabbit IgG(H + L) antibody (926-32211, LI-COR, 1:10,000) according to the manufacturer’s protocol. Blots were stained with Ponceau S to verify equal loading.
Song T., Zhang Y., Zhang Q., Zhang X., Shen D., Yu J., Yu M., Pan X., Cao H., Yong M., Qi Z., Du Y., Zhang R., Yin X., Qiao J., Liu Y., Liu W., Sun W., Zhang Z., Wang Y., Dou D., Ma Z, & Liu Y. (2021). The N-terminus of an Ustilaginoidea virens Ser-Thr-rich glycosylphosphatidylinositol-anchored protein elicits plant immunity as a MAMP. Nature Communications, 12, 2451.
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