Anti-APC抗体[CC-1]
参阅全部 APC 一抗
小鼠单克隆抗体[CC-1] to APC
Mouse
适用于: Flow Cyt, IHC-P, ICC/IFmore details
与反应: Human
Synthetic peptide corresponding to APC aa 1-226.
Epitope is within amino acid residues 1 - 226 of APC.
Purkinje cells or cerebellum tissue.
APC is well suited for immunohistochemical and immunofluorescence studies of oligodendrocytes and optic nerves due to the antibody’s staining of the cell body as opposed to the myelinated processes.
Although we list several publications demonstrating mouse reactivity, we have also received conflicting data from researchers demonstrating a lack of mouse reactivity. Therefore, we have removed mouse from our list of reactive species and no longer guarantee the product for this species.
This product was changed from ascites to tissue culture supernatant on 17 May 2019. Please note that the dilutions may need to be adjusted accordingly. If you have any questions, please do not hesitate to contact our scientific support team.
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. Upon delivery aliquot. Store at +4°C.
Preservative: 0.05% Sodium azide
Constituents: 0.8766% Sodium chloride, 1.902% Tris glycine
Protein G purified
APC is well suited for immunohistochemical and immunofluorescence studies of oligodendrocytes and optic nerves due to the antibody’s staining of the cell body as opposed to the myelinated processes.
单克隆
CC-1
IgG2b
Abpromise™承诺保证使用ab16794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 |
---|---|---|
Flow Cyt | Use at an assay dependent concentration. ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody. | |
IHC-P | (1) | Use at an assay dependent concentration. Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol. |
ICC/IF | Use at an assay dependent concentration. |
Entrez Gene: 324 Human
Omim: 611731 Human
SwissProt: P25054 Human
Unigene: 158932 Human
APC_HUMAN antibody
CC1 antibody
Deleted in polyposis 2.5 antibody
DP2 antibody
DP2.5 antibody
DP3 antibody
FAP antibody
FPC antibody
GS antibody
Protein APC antibody
Adenomatous Polyposis Coli antibody
Adenomatous polyposis coli protein antibody
Apc antibody
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-APC antibody [CC-1] (ab16794)
IHC analysis of formalin-fixed, paraffin embedded human cerebellum with ab16794.
Antibody was used at a concentration of 2.5 µg/ml and sections were pretreated with heat using a pressure cooker prior to staining. Detection with DAB and hematoxylin as a counterstain.
This image was generated using the ascites version of the product.
Immunocytochemistry/ Immunofluorescence - Anti-APC antibody [CC-1] (ab16794)
ICC/IF image of ab16794 stained HeLa 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 (ab16794, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 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.
This image was generated using the ascites version of the product.
Flow Cytometry - Anti-APC antibody [CC-1] (ab16794)
Overlay histogram showing HCT116 cells stained with ab16794 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab16794, 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 IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HCT116 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
This image was generated using the ascites version of the product.