Anti-PLGF抗体- N-terminal
参阅全部 PLGF 一抗
兔多克隆抗体to PLGF - N-terminal
Rabbit
适用于: WB, ICC/IFmore details
与反应: Human, Recombinant fragment
Synthetic peptide corresponding to Human PLGF (N terminal). Highly purified N-terminal 20 aa synthetic peptide (Human).
Database link: P49763
According to Swissprot P49763; PLGF exists in three isoforms PLGF 1, 2 and 3. The N-terminal immunogen sequence of ab9542 is present in all isoforms so extra bands might be observed near the band of interest.
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Lyophilized:Reconstitute in sterile water to a concentration of 0.1-1.0 mg/ml.
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Constituent: PBS
Protein A purified
多克隆
IgG
Abpromise™承诺保证使用ab9542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 |
---|---|---|
WB | (1) | Use a concentration of 1 - 4 µg/ml. It will detect 25 - 50 ng/lane of recombinant human PLGF-1 (17-18 kDa) and PLGF-2 (22-23 kDa) under reducing conditions. Dimers are detected at higher protein amounts/lane. |
ICC/IF | Use a concentration of 1 µg/ml. |
Entrez Gene: 5228 Human
Omim: 601121 Human
SwissProt: P49763 Human
Unigene: 252820 Human
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Western blot - Anti-PLGF antibody - N-terminal (ab9542)
Western blot of chromatography purified, recombinant PLGF-1/-2 and VEGF165 immobilized to PVDF-membrane.
PlGF antibody shows no cross-reactivity to VEGF165.
Immunocytochemistry/ Immunofluorescence - Anti-PLGF antibody - N-terminal (ab9542)
ICC/IF image of ab9542 stained HepG2 (human liver hepatocellular carcinoma cell line) cells. The cells were fixed in 4% formaldehyde for 10 minutes and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1 hour to permeabilize the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab9542, 1 µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1 hour. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1 hour. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43 µM.
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