Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IF-Tissue |
Clonality: | Monoclonal |
Clone number: | SD08-60 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. 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: 69 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human Cdc23 aa 521-570 / 597. |
Positive control: | Hela cell lysate, Jurkat cell lysate, Hela, HepG2. |
Subcellular location: | Cytosol. |
Recommended Dilutions:
WB IF-Cell IF-Tissue |
1:1,000-1:2,000 1:50-1:200 1:50-1:200 |
Uniprot #: | SwissProt: Q9UJX2 Human | Q8BGZ4 Mouse Unigene: 139314 Rat |
Alternative names: | ANAPC8 Anaphase promoting complex subunit 8 Anaphase-promoting complex subunit 8 Apc 8 APC8 Cdc 23 CDC23 CDC23_HUMAN cell division cycle 23 Cell division cycle 23 homolog Cell division cycle protein 23 Cell division cycle protein 23 homolog Cut23 Cyclosome subunit 8 |
Fig1:
Western blot analysis of CDC23 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1612-84, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Hela cell lysate Lane 2: Jurkat cell lysate |
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Fig2: ICC staining of CDC23 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1612-84, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). | |
Fig3: ICC staining of CDC23 in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1612-84, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). |