Confirmed by Immunoprecipitation (IP)

Sino Biological Inc. hase commit to developing a variety of antibodies, including Immunohistochemistry / IHC antibody, Flow Cytometry / FACS antibody, Immunofluorescence / IF / ICC antibody, Immunoprecipitation / IP antibody, Western Blot / WB antibody and ELISA antibody.

There are a variety of detection methods for antibody, and the method can verify each other. The Immunofluorescence / IF / ICC antibodies can be verified by the method of IHC, FAC(FC) and WB. If one result of IHC,FAC(FC) and WB was correct, Immunofluorescence / IF / ICC antibodies were validated that the the Immunofluorescence / IF / ICC antibody is specific to target.

IF Antibodies Confirmed by Immunoprecipitation / IP

XRCC6 Catalog: 101116-T46


Immunofluorescence staining of ARIH2 in HeLa cells. Cells were fixed with 4% PFA,blocked with 10% serum, and incubated with rabbit anti-human ARIH2 polyclonal antibody (1 µg/ml) at 4℃ overnight. Then cells were stained with the Alexa Fluor®488-conjugated Goat Anti-rabbit IgG secondary antibody (green)Positive staining was localized to nucleus.

APEX1 / AP / APEx Catalog: 100801-T46


Immunofluorescence staining of APEX1 in HeLa cells. Cells were fixed with 4% PFA,blocked with 10% serum, and incubated with rabbit anti-human APEX1 polyclonal antibody (1 µg/ml) at 4℃ overnight.

Latexin / LXN Catalog: 10211-R101


Immunofluorescence staining of Human LXN in MCF7 cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with Rabbit anti-Human LXN monoclonal antibody (15 µg/ml) at 4℃ overnight. Then cells were stained with the Alexa Fluor® 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.

ASF1A Catalog: 100840-T38


Immunofluorescence staining of ASF1A in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS,blocked with 10% serum, and incubated with rabbit anti-human ASF1A polyclonal antibody (1 µg/ml) at 4℃ overnight. Then cells were stained with the Alexa Fluor®594-conjugated Goat Anti-rabbit IgG secondary antibody (red)Positive staining was localized to nucleus.