CLPX Recombinant Rabbit Monoclonal Antibody [JE62-96]
cat.: HA721016
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P
Clonality: Monoclonal
Clone number: JE62-96
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 69 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human CLPX aa 584-633/633.
Positive control: Raji cell lysate, Hela cell lysate, HepG2 cell lysate, NIH/3T3 cell lysate, rat heart tissue lysate, mouse heart tissue lysate, mouse liver tissue lysate, rat liver tissue lysate, rat testis tissue, mouse stomach tissue, NCI-H441.
Subcellular location: Mitochondrion, mitochondrion nucleoid.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P

1:500
1:50
1:100-1:400
Uniprot #: SwissProt: O76031 Human | Q9JHS4 Mouse | Q5U2U0 Rat
Alternative names: ATP dependent Clp protease ATP binding subunit clpX like, mitochondrial ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial AU014732 Caseinolytic mitochondrial matrix peptidase chaperone subunit Caseinolytic peptidase X (E.coli) Caseinolytic protease X clpX ClpX caseinolytic peptidase X homolog ClpX caseinolytic protease X homolog CLPX_HUMAN E330029I21 Energy dependent regulator of proteolysis
Images
HA721016_1.jpg Fig1: Western blot analysis of CLPX on different lysates with Rabbit anti-CLPX antibody (HA721016) at 1/500 dilution.

Lane 1: Raji cell lysate
Lane 2: Hela cell lysate
Lane 3: HepG2 cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 69 kDa
Observed band size: 69 kDa

Exposure time: 2 minutes;

10% 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 (HA721016) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
HA721016_2.jpg Fig2: Western blot analysis of CLPX on different lysates with Rabbit anti-CLPX antibody (HA721016) at 1/500 dilution.

Lane 1: NIH/3T3 cell lysate, 10 µg/Lane
Lane 2: Rat heart tissue lysate, 20 µg/Lane
Lane 3: Mouse heart tissue lysate, 20 µg/Lane
Lane 4: Mouse liver tissue lysate, 20 µg/Lane
Lane 5: Rat liver tissue lysate, 20 µg/Lane

Predicted band size: 69 kDa
Observed band size: 69 kDa

Exposure time: 2 minutes;

8% 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 (HA721016) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
HA721016_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat testis tissue with Rabbit anti-CLPX antibody (HA721016) at 1/100 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 (HA721016) at 1/100 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.
HA721016_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse stomach tissue with Rabbit anti-CLPX antibody (HA721016) at 1/400 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 (HA721016) at 1/400 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.
HA721016_5.jpg Fig5: Immunocytochemistry analysis of NCI-H441 cells labeling CLPX with Rabbit anti-CLPX antibody (HA721016) at 1/50 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-CLPX antibody (HA721016) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 647, HA1127) were used as the secondary antibody at 1/1,000 dilution.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.