Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).| Product Name | DP1 [JE52-55] |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | DP 1 antibody DP1 antibody DRTF1 antibody DRTF1-polypeptide 1 antibody E2F dimerization partner 1 antibody E2F related transcription factor antibody TFDP1 antibody TFDP1_HUMAN antibody Transcription factor Dp-1 antibody Transcription factor sequence-specific, DRTF1 antibody |
| Product description | This gene encodes a member of a family of transcription factors that heterodimerize with E2F proteins to enhance their DNA-binding activity and promote transcription from E2F target genes. The encoded protein functions as part of this complex to control the transcriptional activity of numerous genes involved in cell cycle progression from G1 to S phase. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 1, 15, and X. E2F factors bind to DNA as homodimers or heterodimers in association with dimerization partner DP1. TFDP1 may be the first example of a family of related transcription factors. |
| Immunogen | Synthetic peptide within C terminal human DP1. |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG |
| Host Species | Recombinant rabbit |
| Tested Applications | WBIHC-PFC |
| WB:1:500-1:2,000: IHC-P:1:50-1:200: FC:1:50-1:100: |
|
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Alternative Names | DP 1 antibody
DP1 antibody
DRTF1 antibody DRTF1-polypeptide 1 antibody E2F dimerization partner 1 antibody E2F related transcription factor antibody TFDP1 antibody TFDP1_HUMAN antibody Transcription factor Dp-1 antibody Transcription factor sequence-specific DRTF1 antibody |
|---|---|
| Molecular Weight(MW) | 45 kDa |
| Cellular Localization | Nucleus, cytoplasm. |
Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Application
Fig5: Flow cytometric analysis of DP1 was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7110-43, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).| Positive Control | SiHa cell lysate, SH-SY5Y cell lysate, mouse thymus tissue lysate, rat large intestine tissue, human lung carcinoma tissue, mouse colon tissue, THP-1. |
|---|---|
| Application Notes | WB:1:500-1:2,000: IHC-P:1:50-1:200: FC:1:50-1:100: |
| Form | Liquid |
|---|---|
| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | 1*TBS (pH7.4), 1%BSA, 50%Glycerol. Preservative: 0.05% Sodium Azide. |
