Anti-M6PR (cation independent)抗体[2G11]
参阅全部 M6PR (cation independent) 一抗
小鼠单克隆抗体[2G11] to M6PR (cation independent)
Mouse
适用于: ICC/IF, Flow Cyt (Intra)more details
不适用于: WB
与反应: Human
预测可用于: Mouse, Rat, Cow, Non human primates, African green monkey不与反应: Hamster
Full length protein. This information is proprietary to Abcam and/or its suppliers.
This antibody is shown to recognize an epitope in the extracellular domain of Mannose 6 Phosphate Receptor.
Flow Cyt (Intra): A431 cells. ICC/IF: HAP1 cells (HAP1-IGF2R knockout cells used as negative cell line).
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
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.
pH: 7.40
Preservative: 0.02% Sodium azide
Constituents: PBS, 6.97% L-Arginine
Ammonium Sulphate Precipitation
单克隆
2G11
IgG2a
Abpromise™承诺保证使用ab2733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 | (15) | Use a concentration of 1 - 10 µg/ml. |
Flow Cyt (Intra) | Use 1µg for 106 cells. ab170191 - Mouse monoclonal IgG2a, is suitable for use as an isotype control with this antibody. |
应用说明
Is unsuitable for WB.
Entrez Gene: 3482 Human
Entrez Gene: 16004 Mouse
Omim: 147280 Human
SwissProt: P11717 Human
SwissProt: Q07113 Mouse
Unigene: 487062 Human
Unigene: 673278 Human
Unigene: 26553 Mouse
Unigene: 486511 Mouse
300 kDa mannose 6 phosphate receptor antibody
300 kDa mannose 6-phosphate receptor antibody
Cation independent mannose 6 phosphate receptor antibody
Cation-independent mannose-6-phosphate receptor antibody
CD222 antibody
CD222 antigen antibody
CI Man 6 P receptor antibody
CI Man-6-P receptor antibody
CI MPR antibody
CI-M6PR antibody
CI-MPR antibody
CIMPR antibody
IGF 2 receptor antibody
IGF 2R antibody
IGF II receptor antibody
IGF-II receptor antibody
IGF2 receptor antibody
Igf2r antibody
Insulin like growth factor 2 receptor antibody
Insulin like growth factor II receptor antibody
Insulin-like growth factor 2 receptor antibody
Insulin-like growth factor II receptor antibody
M6P R antibody
M6P/IGF2 receptor antibody
M6P/IGF2R antibody
M6PR antibody
mannose 6 phosphate receptor antibody
mannose 6 phosphate receptor, cation independent antibody
MPR 300 antibody
MPR300 antibody
MPRI antibody
MPRI_HUMAN antibody
Immunocytochemistry/ Immunofluorescence - Anti-M6PR (cation independent) antibody [2G11] (ab2733)
ab2733 staining IGF2R in wild-type HAP1 cells (top panel) and IGF2R knockout HAP1 cells (bottom panel). The cells were fixed with 100% methanol (5min), permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with ab2733 at 1ug/ml and ab6046 (Tubulin) at 1/1000 dilution overnight at +4°C, followed by a further incubation at room temperature for 1h with a goat secondary antibody to mouse IgG (Alexa Fluor® 488) (ab150117) at 2 μg/ml (shown in green) and a goat secondary antibody to rabbit IgG (Alexa Fluor® 594) (ab150080) at 2 μg/ml (shown in pseudo color red). Nuclear DNA was labelled in blue with DAPI.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Immunocytochemistry/ Immunofluorescence - Anti-M6PR (cation independent) antibody [2G11] (ab2733)
ICC/IF image of ab2733 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab2733, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 WGA was used to label plasma membranes (red).
Flow Cytometry (Intracellular) - Anti-M6PR (cation independent) antibody [2G11] (ab2733)
Overlay histogram showing HeLa cells stained with ab2733 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab2733, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
Immunocytochemistry/ Immunofluorescence - Anti-M6PR (cation independent) antibody [2G11] (ab2733)Luke Hughes-Davies and Rhiannon Jade, Gurdon Institute, Cambridge, UK
Immunofluorescent imaging of human cells (U2OS) with ab2733 confirms the specificity of this antibody, with the expected perinuclear vesicular staining of lysosomes.
IF was performed with a standard paraformaldehyde technique (fixed in PBS buffered PFH 4% for 5 minutes, permeabilised with 0.5% triton-PBS for 5 minutes, blocked with 5% milk / 0.2% tween for one hour. Primary antibody used at 1/100 in 5% milk / 0.2% TWEEN for one hour, secondary antibody for 30 minutes. All blocking and incubation steps carried out at 37 degrees.
Immunocytochemistry/ Immunofluorescence - Anti-M6PR (cation independent) antibody [2G11] (ab2733)
ab2733 positively staining formaldehyde fixed Human HEK 293 cells (red) in conjunction with goat anti mouse (Alexa 546). Nuclear staining was obtained using Hoechst.
This image is an edited version of an image received courtesy of an Abreview submitted by Kun Liu on 19 September 2005. We do not have any further information relating to this image.
Immunocytochemistry/ Immunofluorescence - Anti-M6PR (cation independent) antibody [2G11] (ab2733)
ICC/IF image of ab2733 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab2733, 10µg/ml) overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti-mouse IgG - H&L, pre-adsorbed (ab96879) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.