Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IF-Cell |
Clonality: | Monoclonal |
Clone number: | JE60-47 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. 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: 35 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human MyoD1 aa 1-100 / 320. |
Positive control: | RD cell lysate, RD. |
Subcellular location: | Nucleus. |
Recommended Dilutions:
WB IF-Cell |
1:1,000 1:100 |
Uniprot #: | SwissProt: P15172 Human |
Alternative names: | bHLHc1 Class C basic helix-loop-helix protein 1 MYF 3 Myf-3 MYF3 Myoblast determination protein 1 Myod 1 MYOD MYOD1 MYOD1_HUMAN Myogenic differentiation 1 Myogenic factor 3 Myogenic factor MYF 3 Myogenin D1 PUM |
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Fig1:
Western blot analysis of MyoD1 on different lysates with Rabbit anti-MyoD1 antibody (HA722179) at 1/1,000 dilution. Lane 1: RD cell lysate Lane 2: HEK-293 cell lysate (negative) Lane 3: HeLa cell lysate (negative) Lane 4: RD cell lysate Lysates/proteins at 30 µg/Lane. Predicted band size: 35 kDa Observed band size: 45 kDa Exposure time: 10 seconds; ECL: K1801; 4-20% 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 (HA722179) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunocytochemistry analysis of RD (positive) and HEK-293 (negative) labeling MyoD1 with Rabbit anti-MyoD1 antibody (HA722179) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-MyoD1 antibody (HA722179) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. |