Anti-RASA1抗体[B4F8]
参阅全部 RASA1 一抗
小鼠单克隆抗体[B4F8] to RASA1
Mouse
This antibody is specific for RASA1 (an alternate name of GAP).
适用于: ICC/IF, WBmore details
与反应: Mouse, Human
预测可用于: Non human primates
Recombinant full length protein corresponding to Human RASA1.
Epitope mapping studies suggest that this antibody binds a portion of GAP that contains the src homology regions SH2 and SH3.
ICC: C2C12, HeLa, A431; WB: HeLa, A431, mouse brain lysate
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Liquid
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.
浓度
100 µg 浓度为 1 mg/ml
Protein A purified
GTPase Activating Protein (GAP) is capable of stimulating the hydrolysis of GTP by ras p21 proteins, though GAP has little effect on the oncogenic forms of ras. It is also known that several tyrosine kinases such as platelet derived growth factor receptor and epidermal growth factor receptor are involved in the tyrosine phosphorylation of GAP. It has therefore been suggested that GAP may provide a connection or link between growth factor receptors and the ras p21 family.
单克隆
B4F8
IgG2a
Abpromise™承诺保证使用ab2922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 |
---|---|---|
ICC/IF | Use a concentration of 5 µg/ml. Immunofluorescence staining of GAP in mouse fibroblast cells results in diffuse cytoplasmic staining. Following the addition of PDGF, immunofluorescence staining shows that some GAP rapidly translocates to the plasma membrane. Read More | |
WB | Use a concentration of 10 µg/ml. By Western blot, this antibody recognizes a single 120 kDa protein representing ras GAP from RS-2 cell lysate. |
Entrez Gene: 5921 Human
Entrez Gene: 218397 Mouse
Omim: 139150 Human
SwissProt: P20936 Human
Unigene: 664080 Human
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Immunocytochemistry/ Immunofluorescence - Anti-RASA1 antibody [B4F8] (ab2922)
ab2922 labelling GAP (green) in the cytoplasm of A431 cells (right) compared with a negative control (left) by Immunocytochemistry/Immunofluorescence. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes, blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4 ºC. A DyLight 488-conjugated Goat anti-mouse IgG (H+L) was used as the secondary antibody. Red (phalloidin) - F-actin, Bue (DAPI) - nuclei. Images were taken at a magnification of 60x.
Immunocytochemistry/ Immunofluorescence - Anti-RASA1 antibody [B4F8] (ab2922)
ab2922 labelling GAP (green) in the cytoplasm of C2C12 cells (right) compared with a negative control (left) by Immunocytochemistry/Immunofluorescence. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes, blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4 ºC. A DyLight 488-conjugated Goat anti-mouse IgG (H+L) was used as the secondary antibody. Red (phalloidin) - F-actin, Bue (DAPI) - nuclei. Images were taken at a magnification of 60x.
Immunocytochemistry/ Immunofluorescence - Anti-RASA1 antibody [B4F8] (ab2922)
ab2922 labelling GAP (green) in the cytoplasm of Hela cells (right) compared with a negative control (left) by Immunocytochemistry/Immunofluorescence. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes, blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4 ºC. A DyLight 488-conjugated Goat anti-mouse IgG (H+L) was used as the secondary antibody. Red (phalloidin) - F-actin, Bue (DAPI) - nuclei. Images were taken at a magnification of 60x.
Western blot - Anti-RASA1 antibody [B4F8] (ab2922)
All lanes : Anti-RASA1 antibody [B4F8] (ab2922) at 1/200 dilution
Lane 1 : HeLa cell lysate
Lane 2 : A431 cell lysate
Lane 3 : Mouse brain cell lysate
Lysates/proteins at 25 µg per lane.
Observed band size: 110 kDawhy is the actual band size different from the predicted?
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