TOMM20 Recombinant Rabbit Monoclonal Antibody [ST04-72] - BSA and Azide free

☑ Relative expression (RE)

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Western blot analysis of TOMM20 on different lysates with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution.

Lane 1: HeLa cell lysate (15 µg/Lane)
Lane 2: Saos-2 cell lysate (low expression) (15 µg/Lane)
Lane 3: HepG2 cell lysate (15 µg/Lane)
Lane 4: A549 cell lysate (15 µg/Lane)
Lane 5: NIH/3T3 cell lysate (15 µg/Lane)
Lane 6: C2C12 cell lysate (15 µg/Lane)
Lane 7: C6 cell lysate (15 µg/Lane)
Lane 8: PC-12 cell lysate (15 µg/Lane)
Lane 9: Mouse brain tissue lysate (30 µg/Lane)
Lane 10: Rat brain tissue lysate (30 µg/Lane)

Predicted band size: 16 kDa
Observed band size: 16 kDa

Exposure time: 3 minutes; ECL: K1801;
4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1609-25) at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution were used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

☑ Knockdown (KD)

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Western blot analysis of TOMM20 on different lysates with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/5,000 dilution.

Lane 1: HeLa-si NT cell lysate (10 µg/Lane)
Lane 2: HeLa-si TOMM20 cell lysate (10 µg/Lane)

Predicted band size: 16 kDa
Observed band size: 16 kDa

Exposure time: 21 seconds; ECL: K1801;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1609-25) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

☑ Relative expression (RE)

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Western blot analysis of TOMM20 on different lysates with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/5,000 dilution.

Lane 1: HeLa cell lysate (10 µg/Lane)
Lane 2: Saos-2 cell lysate (low expression) (10 µg/Lane)
Lane 3: HepG2 cell lysate (10 µg/Lane)
Lane 4: A549 cell lysate (10 µg/Lane)
Lane 5: MCF7 cell lysate (10 µg/Lane)
Lane 6: NIH/3T3 cell lysate (10 µg/Lane)
Lane 7: F9 cell lysate (10 µg/Lane)
Lane 8: PC-12 cell lysate (10 µg/Lane)
Lane 9: Mouse brain tissue lysate (20 µg/Lane)
Lane 10: Rat brain tissue lysate (20 µg/Lane)
Lane 11: Rat lung tissue lysate (20 µg/Lane)

Predicted band size: 16 kDa
Observed band size: 16 kDa

Exposure time: 1 minute 22 seconds; ECL: K1801;
4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1609-25) at 1/5,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/100,000 dilution was used for 1 hour at room temperature.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Application: IF-cell

Species: Human

Cell Sample: HeLa cell

Antibody concentration: 1: 1,000

Data by conrtesy of: Mr. Wenxiang Huang
School of Basic Medical Sicences, Zhejiang University

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Application: IF-cell

Species: Human

Cell Sample: AC16 cell

Antibody concentration: 1: 200

Data by conrtesy of: Mr. Zhiyi Yang
School of Basic Medical Sicences, Zhejiang University

☑ Relative expression (RE)

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HepG2 (high expression) and Saos-2 (low expression) labeling TOMM20 with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/1,000 dilution and competitor's antibody at 1/400 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/1,000 dilution and competitor's antibody at 1/400 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of NIH/3T3 cells labeling TOMM20 with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/1,000 dilution and competitor's antibody at 1/400 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/1,000 dilution and competitor's antibody at 1/400 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HeLa cells labeling TOMM20 with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/1,000 dilution.

Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/1,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Counterstained with Mitotracker. Nuclear DNA was labelled in blue with DAPI.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/500 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH₂O and PBS, and then probed with the primary antibody (ET1609-25) at 1/500 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat kidney tissue with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/500 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH₂O and PBS, and then probed with the primary antibody (ET1609-25) at 1/500 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/500 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH₂O and PBS, and then probed with the primary antibody (ET1609-25) at 1/500 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/800 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH₂O and PBS, and then probed with the primary antibody (ET1609-25) at 1/800 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat large intestine tissue with Rabbit anti-TOMM20 antibody (ET1609-25) at 1/800 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH₂O and PBS, and then probed with the primary antibody (ET1609-25) at 1/800 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Application: IHC-Fr

Species: Mouse

Site: Kidney

Sample: Frozen section

Antibody concentration: 1/500

Antigen retrieval: Not required

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Application: IHC-Fr

Species: Rat

Site: Kidney

Sample: Frozen section

Antibody concentration: 1/500

Antigen retrieval: Not required

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
TOMM20 was immunoprecipitated in 0.2mg HeLa cell lysate with ET1609-25 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using ET1609-25 at 1/1,000 dilution. Anti-Rabbit IgG for IP, AlpSdAbs® VHH(HRP) (025-100-005) at 1/5,000 dilution was used for 1 hour at room temperature.

Lane 1: HeLa cell lysate (input)
Lane 2: Rabbit IgG instead of ET1609-25 in HeLa cell lysate
Lane 3: ET1609-25 IP in HeLa cell lysate

Blocking/Dilution buffer: 5% NFDM/TBST
Exposure time: 1 minute 2 seconds

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of HeLa cells labeling TOMM20.

Cells were fixed and permeabilized. Then stained with the primary antibody (ET1609-25, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Application: Immunofluorescence (IF-tissue)

Species: Mouse
Tissue: kidney
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95℃.

Wash buffer: 1× PBS
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: ET1609-25, 1/500, overnight at 4℃.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 1.5 hours at room temperature.

This data was developed using ET1609-25, the same antibody clone in a different buffer formulation.
Application: Immunofluorescence (IF-tissue)

Species: Rat
Tissue: brain
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95℃.

Wash buffer: 1× PBS
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: ET1609-25, 1/500, overnight at 4℃.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 1.5 hours at room temperature.