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: | JE52-36 |
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: 107 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human ERAP1 aa 833-941 / 941. |
Positive control: | A431 cell lysate, PC-12 cell lysate, Mouse heart tissue lysate, Rat liver tissue lysate, human placenta tissue. |
Subcellular location: | Endoplasmic reticulum membrane. |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:1,000 |
Uniprot #: | SwissProt: Q9NZ08 Human | Q9EQH2 Mouse | Q9JJ22 Rat |
Alternative names: | A LAP A-LAP Adipocyte derived leucine aminopeptidase Adipocyte-derived leucine aminopeptidase ALAP Aminopeptidase PILS Aminopeptidase regulator of TNFR1 shedding APPILS ARTS 1 ARTS-1 Arts1 Endoplasmic reticulum aminopeptidase 1 Endoplasmic reticulum aminopeptidase associated with antigen processing ERAAP ERAAP1 ERAP 1 Erap1 ERAP1_HUMAN KIAA0525 kiaa0525 protein PILS AP PILS-AP PILSA PILSAP Puromycin insensitive leucyl specific aminopeptidase Puromycin-insensitive leucyl-specific aminopeptidase Type 1 tumor necrosis factor receptor shedding aminopeptidase regulator type 1 tumor necrosis factor receptors shedding aminopeptidase regulator VEGF-induced aminopeptidase |
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Fig1:
All lanes: Western blot analysis of ERAP1 with anti-ERAP1 antibody [JE52-36] (ET7110-29) at 1/500 dilution. Lane 1: Wild-type 293T whole cell lysate. Lane 2: ERAP1 knockout 293T whole cell lysate. ET7110-29 was shown to specifically react with ERAP1 in wild-type 293T cells. No band was observed when ERAP1 knockout sample was tested. Wild-type and ERAP1 knockout samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary Anti-ERAP1 antibody (ET7110-29, 1/500) and Anti-β-actin antibody (R1207-1, 1/1,000) were used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG H&L (HRP) Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. Cell lysate was provided by Ubigene Biosciences (Ubigene Biosciences Co., Ltd., Guangzhou, China). |
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Fig2:
Western blot analysis of ERAP1 on different lysates with Rabbit anti-ERAP1 antibody (ET7110-29) at 1/1,000 dilution. Lane 1: A431 cell lysate (20 µg/Lane) Lane 2: PC-12 cell lysate (20 µg/Lane) Lane 3: Mouse heart tissue lysate (40 µg/Lane) Lane 4: Rat liver tissue lysate (40 µg/Lane) Predicted band size: 107 kDa Observed band size: 107 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 (ET7110-29) 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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Fig3:
Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-ERAP1 antibody (ET7110-29) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (ET7110-29) 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. |