WB
Western blot analysis of lysates from wild type (WT) and LDL Receptor (LDLR) knockout (KO) HeLa cells
using [KO Validated] LDL Receptor (LDLR) Rabbit pAb at 1:5000 dilution incubated overnight
at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 90 s.
WB
Western blot analysis of various lysates using [KO Validated] LDL Receptor (LDLR) Rabbit pAb
at 1:5000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 45 s.
IHC
Immunohistochemistry analysis of paraffin
embedded Mouse lung tissue using [KO
Validated] LDL Receptor (LDLR) Rabbit pAb at a dilution of 1:600 (40x lens).
High pressure antigen retrieval performed
with 0.01M Tris-EDTA Buffer (pH 9.0) prior to
IHC staining.
IHC
Immunohistochemistry analysis of paraffin
embedded Rat brain tissue using [KO
Validated] LDL Receptor (LDLR) Rabbit pAb
at a dilution of 1:600 (40x lens).
High pressure antigen retrieval performed
with 0.01M Tris-EDTA Buffer (pH 9.0) prior to
IHC staining.
ICC/IF
Confocal imaging of Hep G2 cells using [KO
Validated] LDL Receptor (LDLR) Rabbit pAb
(dilution 1:300) followed by a
further incubation with Cy3-conjugated Goat
anti-Rabbit IgG (H+L) (dilution 1:500)
(Red). The cells were counterstained with α
Tubulin Mouse mAb (dilution 1:400)
followed by incubation with 488
conjugated Goat Anti-Mouse IgG (H+L) Ab
(dilution 1:500) (Green). DAPI was
used for nuclear staining (Blue). Objective:
100x.