Product Type: | Mouse monoclonal IgG1, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | A3F9 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 2ug/ul |
Purification: | Protein G affinity purified. |
Molecular weight: | Predicted band size: 37 kDa |
Isotype: | IgG1 |
Immunogen: | Recombinant protein within human CD1A aa 50-250. |
Positive control: | K562 cell lysates, human skin tissue. |
Subcellular location: | Cell membrane, endosome membrane, membrane raft. |
Recommended Dilutions:
WB IHC-P |
1:500-1:1,000 1:1,000 |
Uniprot #: | SwissProt: P06126 Human |
Alternative names: | CD 1a CD1 CD1a CD1A Antigen CD1A antigen, a polypeptide CD1a molecule CD1A_HUMAN cluster of differentiation 1 A cortical thymocyte antigen CD1A differentiation antigen CD1 alpha 3 epidermal dendritic cell marker CD1a FCB 6 FCB6 HTA 1 HTA1 hTa1 thymocyte antigen OTTHUMP00000018907 R 4 R4 T 6 T-cell surface antigen T6/Leu-6 T-cell surface glycoprotein CD1a T6 |
Fig1: Western blot analysis of CD1A on K562 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (EM1901-89, 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. | |
Fig2:
Immunohistochemical analysis of paraffin-embedded human skin tissue with Mouse anti-CD1A antibody (EM1901-89) 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 (EM1901-89) 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. |