Product Type: | Mouse monoclonal IgG2b, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P, IF-Cell |
Clonality: | Monoclonal |
Clone number: | A9H9 |
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: 84 kDa |
Isotype: | IgG2b |
Immunogen: | Recombinant protein within human PSMA aa 20-750 / 750. |
Positive control: | LNCaP cell lysate, 22RV1 cell lysate, human prostate tissue, human prostate carcinoma tissue, LNCaP. |
Subcellular location: | Cell membrane, Cytoplasm. |
Recommended Dilutions:
WB IHC-P IF-Cell |
1:1,000 1:1,000 1:100 |
Uniprot #: | SwissProt: Q04609 Human |
Alternative names: | Cell growth inhibiting protein 27 Cell growth-inhibiting gene 27 protein FGCP Folate hydrolase (prostate-specific membrane antigen) 1 Folate hydrolase 1 Folate hydrolase Folate hydrolase prostate specific membrane antigen 1 FOLH 1 FOLH Folh1 FOLH1_HUMAN Folylpoly gamma glutamate carboxypeptidase Folylpoly-gamma-glutamate carboxypeptidase GCP 2 GCP II GCP2 GCPII GIG27 Glutamate carboxylase II Glutamate carboxypeptidase 2 Glutamate carboxypeptidase II Membrane glutamate carboxypeptidase mGCP N acetylated alpha linked acidic dipeptidase 1 N-acetylated-alpha-linked acidic dipeptidase I NAALAD 1 NAALAD1 NAALAdase NAALADase I Prostate specific membrane antigen Prostate specific membrane antigen variant F Prostate-specific membrane antigen PSM PSMA Pteroylpoly gamma glutamate carboxypeptidase Pteroylpoly-gamma-glutamate carboxypeptidase |
Fig1:
Western blot analysis of PSMA on different lysates with Mouse anti-PSMA antibody (HA601164) at 1/1,000 dilution. Lane 1: LNCaP cell lysate Lane 2: 22RV1 cell lysate Lane 3: PC-3M cell lysate (negative) Lysates/proteins at 20 µg/Lane. Predicted band size: 84 kDa Observed band size: 100/200 kDa Exposure time: 2 minutes 10 seconds; 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 (HA601164) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/100,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunocytochemistry analysis of LNCaP (positive) and PC-3M (negative) cells labeling PSMA with Mouse anti-PSMA antibody (HA601164) at 1/100 dilution. Cells were fixed in 100% precooled methanol 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 Mouse anti-PSMA antibody (HA601164) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) 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 (ET1602-4, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594, HA1122) were used as the secondary antibody at 1/1,000 dilution. |
Fig3:
Immunohistochemical analysis of paraffin-embedded human prostate tissue with Rabbit anti-PSMA antibody (HA601164) 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 (HA601164) 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 human prostate carcinoma tissue with Rabbit anti-PSMA antibody (HA601164) 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 (HA601164) 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. |