Connexin 46 Antibody(UPA02962)

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

Basic information
Catalog No.:UPA02962
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 (1:50 - 1:100), IF/ICC (1:50 - 1:200)
Reactivity:
Human,Mouse,Rat,Dog
Specificity:
Recognizes endogenous levels of Connexin 46 protein.
Immunogen:
KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Connexin 46. The exact sequence is proprietary.
Description:
Rabbit polyclonal antibody to Connexin 46
Uniprot:
Q9Y6H8
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:
GJA3; Gap junction alpha-3 protein; Connexin-46; Cx46
Data:
Western blot analysis of Connexin 46 expression in A549 (A), U2OS (B), DLD (C), mouse heart (D), rat heart (E) whole cell lysates. (Predicted band size: 47 kD; Observed band size: 53 kD)
Immunohistochemical analysis of Connexin 46 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 Connexin 46 staining in A549 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 hidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
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