LMO2 Recombinant Rabbit Monoclonal Antibody [PD00-25]
cat.: HA721212
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: PD00-25
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 18 kDa
Isotype: IgG
Immunogen: Recombinant protein full length human LMO2.
Positive control: K562 cell lysates, mouse brain tissue, human tonsil tissue, human lymph nodes tissue.
Subcellular location: Nucleus.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:1,000-1:2000
Uniprot #: SwissProt: P25791 Human | P25801 Mouse
Alternative names: Cysteine rich protein TTG 2 Cysteine rich protein TTG2 Cysteine-rich protein TTG-2 LIM domain only 2 (rhombotin like 1) LIM domain only 2 LIM domain only protein 2 LMO 2 LMO-2 lmo2 RBTN 2 RBTN L1 RBTN2 RBTN2_HUMAN RBTNL 1 RBTNL1 RHOM 2 RHOM2 Rhombotin 2 Rhombotin like 1 Rhombotin-2 Rhombotin2 T cell translocation gene 2 T cell translocation protein 2 T-cell translocation protein 2 TTG 2 TTG2
Images
HA721212_1.jpg Fig1: Western blot analysis of LMO2 on K562 cell lysates with Rabbit anti-LMO2 antibody (HA721212) at 1/1,000 dilution.

Lysates/proteins at 10 µg/Lane.

Predicted band size: 18 kDa
Observed band size: 18 kDa

Exposure time: 2 minutes;

15% 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 (HA721212) 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 1:300,000 dilution was used for 1 hour at room temperature.
HA721212_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-LMO2 antibody (HA721212) at 1/1,000 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 (HA721212) at 1/1,000 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.
HA721212_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-LMO2 antibody (HA721212) at 1/2,000 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 (HA721212) at 1/2,000 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.
HA721212_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human lymph nodes tissue with Rabbit anti-LMO2 antibody (HA721212) at 1/2,000 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 (HA721212) at 1/2,000 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”.