HLTF Recombinant Rabbit Monoclonal Antibody [JE35-59]
cat.: HA722329
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | WB, IF-Cell, IHC-P |
| Clonality: | Monoclonal |
| Clone number: | JE35-59 |
| 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: 114 kDa |
| Isotype: | IgG |
| Immunogen: | Recombinant protein within Human HLTF aa 910-1,009 / 1,009. |
| Positive control: | HeLa cell lysate, K-562 cell lysate, HCT 116 cell lysate, HeLa, human ovary cancer tissue, human testis tissue. |
| Subcellular location: | Cytoplasm, Nucleus, nucleolus, nucleoplasm. |
| Recommended Dilutions:
WB IF-Cell IHC-P |
1:2,000 1:100 1:200-1:1,000 |
| Uniprot #: | SwissProt: Q14527 Human |
| Alternative names: | DNA-binding protein/plasminogen activator inhibitor 1 regulator Helicase like transcription factor Helicase-like transcription factor HIP116 HIP116A HLTF 1 Hltf HLTF_HUMAN HLTF1 p113 RING finger protein 80 RNF80 SMARC A3 SMARCA 3 SMARCA3 SNF2-like 3 SNF2L3 Sucrose nonfermenting protein 2 like 3 Sucrose nonfermenting protein 2-like 3 SWI/SNF related matrix associated actin dependent regulator of chromatin subfamily A member 3 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin a3 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 3 ZBU 1 ZBU1 |
Images
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Fig1:
Western blot analysis of HLTF on different lysates with Rabbit anti-HLTF antibody (HA722329) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: K-562 cell lysate Lane 3: HCT 116 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 114 kDa Observed band size: 114 kDa Exposure time: 25 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 (HA722329) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunocytochemistry analysis of HeLa cells labeling HLTF with Rabbit anti-HLTF antibody (HA722329) at 1/100 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-HLTF antibody (HA722329) at 1/100 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. |
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Fig3:
Immunohistochemical analysis of paraffin-embedded human ovary cancer tissue with Rabbit anti-HLTF antibody (HA722329) 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 (HA722329) 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. |
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Fig4:
Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-HLTF antibody (HA722329) 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 (HA722329) 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. |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.