HRPT2 Recombinant Rabbit Monoclonal Antibody [JE66-42]
cat.: HA721390
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE66-42
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: 61 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human HRPT2 aa 331-430 / 531.
Positive control: SW480 cell lysate, K-562 cell lysate, HeLa cell lysate, Jurkat cell lysate, HepG2 cell lysate, MCF7 cell lysate, HEK-293 cell lysate, RAW264.7 cell lysate, human kidney tissue, human testis tissue, rat kidney tissue.
Subcellular location: Nucleus.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:200
Uniprot #: SwissProt: Q6P1J9 Human | Q8JZM7 Mouse | Q4V8C8 Rat
Alternative names: C1orf28 CDC 73 Cdc73 CDC73_HUMAN Cell division cycle 73 Cell division cycle 73 Paf1/RNA polymerase II complex component homolog Cell division cycle 73 Paf1/RNA polymerase II complex component like protein Cell division cycle protein 73 homolog FIHP FLJ23316 HPT JT HPTJT HRPT 2 HRPT1 HRPT2 Hyperparathyroidism 2 (with jaw tumor) Hyperparathyroidism 2 Hyperparathyroidism 2 protein HYX Paf1/RNA polymerase II complex component Parafibromin
Images
HA721390_1.jpg Fig1: Western blot analysis of HRPT2 on different lysates with Rabbit anti-HRPT2 antibody (HA721390) at 1/1,000 dilution.

Lane 1: SW480 cell lysate
Lane 2: K-562 cell lysate
Lane 3: HeLa cell lysate
Lane 4: Jurkat cell lysate
Lane 5: HepG2 cell lysate
Lane 6: MCF7 cell lysate
Lane 7: HEK-293 cell lysate
Lane 8: RAW264.7 cell lysate

Lysates/proteins at 15 µg/Lane.

Predicted band size: 61 kDa
Observed band size: 61 kDa

Exposure time: 3 minutes;

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 (HA721390) at 1/1,000 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.
HA721390_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-HRPT2 antibody (HA721390) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (HA721390) at 1/200 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.
HA721390_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-HRPT2 antibody (HA721390) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (HA721390) at 1/200 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.
HA721390_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat kidney tissue with Rabbit anti-HRPT2 antibody (HA721390) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (HA721390) at 1/200 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.