Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JA10-63 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. 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: 23 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human Lin28A aa 10-59 / 209. |
Positive control: | NCCIT cell lysates, JAR cell lysate, human testis tissue, mouse placenta tissue, rat testis tissue. |
Subcellular location: | Cytoplasm. Nucleus. |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:400-1:1,000 |
Uniprot #: | SwissProt: Q9H9Z2 Human | Q8K3Y3 Mouse | D3ZZA6 Rat |
Alternative names: | AL024421 CSDD1 CSDD2 FLJ12457 Lin 28 Lin 28 homolog (C. elegans) Lin 28 homolog A (C. elegans) Lin 28 homolog A Lin 28 homolog Lin-28A Lin28 Lin28, C. elegans, homolog of, A LIN28A LN28A_HUMAN Protein lin-28 homolog A Protein lin-28 homolog B RNA binding protein lin 28 Tex17 ZCCHC1 Zinc finger CCHC domain containing 1 Zinc finger CCHC domain containing protein 1 Zinc finger CCHC domain-containing protein 1 |
Fig1:
Western blot analysis of Lin28A on NCCIT cell lysates with Rabbit anti-Lin28A antibody (ET1704-26) at 1/1,000 dilution. Lysates/proteins at 20 µg/Lane. Predicted band size: 23 kDa Observed band size: 28 kDa Exposure time: 3 minutes; 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 (ET1704-26) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. 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:
Western blot analysis of Lin28A on different lysates with Rabbit anti-Lin28A antibody (ET1704-26) at 1/1,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: JAR cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 23 kDa Observed band size: 28 kDa Exposure time: 30 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 (ET1704-26) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
Fig3:
Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-Lin28A antibody (ET1704-26) 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 (ET1704-26) 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. |
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Fig4:
Immunohistochemical analysis of paraffin-embedded mouse placenta tissue with Rabbit anti-Lin28A antibody (ET1704-26) 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 (ET1704-26) 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. |
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Fig5:
Immunohistochemical analysis of paraffin-embedded rat testis tissue with Rabbit anti-Lin28A antibody (ET1704-26) at 1/400 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 (ET1704-26) 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. |