Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Zebrafish |
Applications: | WB, IF-Cell, IHC-P |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 41 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human CD34 aa 336-385. |
Positive control: | Human brain, mouse brain, mouse testis, Mouse thymus, mouse spleen, Jurkat, TF-1, F9, human embryonic stem cell, human tonsil tissue |
Subcellular location: | Cell membrane |
Recommended Dilutions:
WB IF-Cell IHC-P |
1:500-1:1,000 1:100 1:3,000 |
Uniprot #: | SwissProt: P28906 Human | Q64314 Mouse |
Alternative names: | CD34 CD34 antigen CD34 molecule CD34_HUMAN Cluster designation 34 Hematopoietic progenitor cell antigen CD34 HPCA1 Mucosialin OTTHUMP00000034733 OTTHUMP00000034734 |
Fig1:
Western blot analysis of CD34 on different cell lysates using anti-CD34 antibody at 1/1,000 dilution. Positive control: Lane 1: Human brain lysate Lane 2: Mouse brain lysate Lane 3: Mouse testis lysate Lane 4: Mouse thymus lysate Lane 5: Mouse spleen lysate Lane 6:Jurkat lysate Lane 7: TF-1 lysate Lane 8: F9 lysate Predicted band size: 41 kDa Observed band size: 90 kDa |
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Fig2: ICC staining of CD34 in hES cells (green). Formalin fixed cells were permeabilized with 0.25% Triton X100/PBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (0108-2, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-CD34 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (0108-2, 1/200) 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. |