Product Type: | Mouse monoclonal IgG1, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | D7-B5 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 2ug/ul |
Purification: | Protein G affinity purified. |
Molecular weight: | 54 kDa |
Isotype: | IgG1 |
Immunogen: | Synthetic peptide within Human CELF2 aa 450-508. |
Positive control: | MCF-7 cell lysate, A549 cell lysate, PC-3M cell lysate, rat brain tissue, mouse brain tissue. |
Subcellular location: | Cytoplasm, Nucleus. |
Recommended Dilutions:
WB IHC-P |
1:500-1:1,000 1:100-1:500 |
Uniprot #: | SwissProt: O95319 Human | Q9Z0H4 Mouse | Q792H5 Rat |
Alternative names: | Bruno-like protein 3 BRUNOL3 Cardiac elav type RNA binding protein CELF-2 celf2 CELF2_HUMAN CUG BP2 CUG triplet repeat RNA-binding protein 2 CUG-BP- and ETR-3-like factor 2 CUG-BP2 CUGBP Elav like family member 2 CUGBP Elav-like family member 2 CUGBP2 dJ323N1.1 elav type RNA binding protein ELAV-type RNA-binding protein 3 ETR 3 ETR-3 ETR3 HGNC:2550 hNAPOR NAPOR 2 NAPOR Neuroblastoma apoptosis-related RNA-binding protein Neuroplastoma apoptosis related RNA binding protein 3 RNA binding protein BRUNOL3 RNA-binding protein BRUNOL-3 |
Fig1:
Western blot analysis of CELF2 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (EM1902-41, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: MCF-7 cell lysate Lane 2: A549 cell lysate Lane 3: PC-3M cell lysate |
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Fig2: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-CELF2 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1902-41, 1/400) for 30 minutes 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. | |
Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-CELF2 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1902-41, 1/400) for 30 minutes 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. |