APAF-1-ALT Antibody(UPA00054)

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50ul598.00
100ul998.00
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Tel: 0550-3721098
antibody@universalbiol.com

Basic information
Catalog No.:UPA00054
Source:Rabbit
Size:50ul/100ul
Clonality:Polyclonal
Concentration:1mg/ml
Isotype:IgG
Purification:The antibody was purified by immunogen affinity chromatography.
Useful information
Applications:
WB (1:500 - 1:1000), IHC (1:100 - 1:200), IF/ICC (1:100 - 1:500)
Reactivity:
Human,Rat
Specificity:
Recognizes endogenous levels of APAF-1-ALT protein.
Immunogen:
KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human APAF-1-ALT. The exact sequence is proprietary.
Description:
Rabbit polyclonal antibody to APAF-1-ALT
Uniprot:
O14727-6
BiowMW:
Refer to Figures
Buffer:
Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% Thimerosal.
Storage:
Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
Note:
For research use only, not for use in diagnostic procedure.
Alternative Name:
APAF1; APAF1-interacting protein; APIP; APIP2; CGI-29 protein; MMRP19; dJ179L10.2; likely ortholog of mouse monocyte macrophage 19
Data:
Western blot analysis of APAF-1-ALT expression in HEK293T (A), PC12 (B) whole cell lysates. (Predicted band size: 37 kD; Observed band size: 37 kD)
Immunohistochemical analysis of APAF-1-ALT staining in human lung cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Immunofluorescent analysis of APAF-1-ALT staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
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