CD1A Mouse Monoclonal Antibody [A4B10]
cat.: HA600031
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human
Applications: IHC-P, FC
Clonality: Monoclonal
Clone number: A4B10
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: Immunogen affinity purified.
Molecular weight: Predicted band size: 37 kDa.
Isotype: IgG1
Immunogen: Recombinant protein within human CD1A aa 50-250 (Extracellular).
Positive control: Human skin tissue, Jurkat.
Subcellular location: Cell membrane, endosome membrane, membrane raft.
Recommended Dilutions:
  IHC-P
  FC

1:100-1:500
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
Images
HA600031_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human skin tissue using anti-CD1A antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) 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 (HA600031, 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.
HA600031_2.jpg Fig2: Flow cytometric analysis of HeLa (left, negative) and Jurkat (right, positive) cells labeling CD1A.

Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA600031, 1/1,000) (red) compared with Mouse IgG1 Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Mouse IgG Secondary antibody (HA1125) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.