Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, FC |
Clonality: | Monoclonal |
Clone number: | PH00-02 |
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: 186 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within C terminal human SET1A. |
Positive control: | 293T cell lysates, 293T, HepG2. |
Subcellular location: | Chromosome, Nucleus |
Recommended Dilutions:
WB FC |
1:1,000 1:500-1:1,000 |
Uniprot #: | SwissProt: O15047 Human | E9PYH6 Mouse | A0A8I6AS32 Rat |
Alternative names: | Histone-lysine N-methyltransferase SETD1A hSET1A KMT2F Lysine N methyltransferase 2F Lysine N-methyltransferase 2F SET domain containing 1A SET domain containing protein 1A SET domain-containing protein 1A SET1 Set1 Ash2 histone methyltransferase complex subunit SET1 Set1/Ash2 histone methyltransferase complex subunit SET1 SET1A SET1A_HUMAN SETD1A |
Fig1:
Western blot analysis of hSET1/SET1 on 293T cell lysates with Rabbit anti-hSET1/SET1 antibody (HA721226) at 1/1,000 dilution. Lysates/proteins at 10 µg/Lane. Predicted band size: 186 kDa Observed band size: 300 kDa Exposure time: 2 minutes; 6% 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 (HA721226) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Flow cytometric analysis of 293T cells labeling hSET1/SET1. Cells were fixed and permeabilized.Then stained with the primary antibody (HA721226, 1ug/ml) (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-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
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Fig3:
Flow cytometric analysis of HepG2 cells labeling hSET1/SET1. Cells were fixed and permeabilized.Then stained with the primary antibody (HA721226, 1ug/ml) (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-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |