驴抗小鼠IgG H&L (HRP)
参阅全部 IgG 二抗
Donkey
Mouse
适用于: Dot blot, ELISA, IHC-P, IHC-Fr, WB, ICC/IFmore details
mouse IgG whole molecule
HRP
Liquid
Shipped at 4°C. Store at +4°C.
Preservative: 0.01% Gentamicin sulphate
Constituents: 1% BSA, 0.424% Potassium phosphate solution, 0.88% Sodium chloride
Affinity purified
This product was prepared from monospecific antiserum by immunoaffinity chromatography using Mouse IgG coupled to agarose.
Horseradish Peroxidase (HRP)
多克隆
IgG
Abpromise™承诺保证使用ab6820于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
Dot blot | Use at an assay dependent concentration. | |
ELISA | 1/70000. | |
IHC-P | 1/500 - 1/2000. | |
IHC-Fr | 1/500 - 1/2000. | |
WB | 1/2000 - 1/10000. | |
ICC/IF | 1/500 - 1/2500. |
Western blot - Donkey Anti-Mouse IgG H&L (HRP) (ab6820)Portegijs et al PLoS Genet. 2016 Oct 6;12(10):e1006291. doi: 10.1371/journal.pgen.1006291. eCollection 2016 Oct. Fig S5. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/
Detection of protein levels in LIN-5 mutants.
(Panel A) Western blots of lysates of yeast clones containing the indicated LIN-5 expression constructs, probed for LIN-5 and tubulin (loading control) levels.
Protein samples were separated on gradient acrylamide gels and subjected to western blotting on polyvinylidene difluoride membrane. Membranes were blocked with 5% skim milk in PBST for 1 hour at room temperature, or overnight at 4°C for stripped blots. For protein detection, primary antibodies used in this study were: mouse anti–LIN-5 (1:1000) and rabbit anti-Tubulin (1:1000, Abcam) for stripped blots. Secondary antibodies used were: donkey anti-mouse HRP (1:5000, Abcam, ab6820) and goat anti-rabbit HRP (1:5000).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Donkey Anti-Mouse IgG H&L (HRP) (ab6820)
IHC image of beta actin staining in human colon formalin fixed paraffin embedded tissue section*.
The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH 6) for 30 mins. The section was incubated with ab8224, 3 µg/ml overnight at +4°C. An HRP-conjugated secondary (ab6820, 1/2000 dilution) was used for 1 hr at room temperature. The section was counterstained with hematoxylin and mounted with DPX.
The inset negative control image is secondary-only at 1/500 dilution.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre