Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IF-Tissue, IP, FC |
Clonality: | Monoclonal |
Clone number: | ST49-07 |
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: | 45 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human PGK1 aa 1-49 / 417. |
Positive control: | Hela cell lysate, MCF-7 cell lysate, HepG2 cell lysate, HepG2, Hela. |
Subcellular location: | Cytoplasm. |
Recommended Dilutions:
WB IF-Cell IF-Tissue FC |
1:1,000-1:5,000 1:50-1:200 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P00558 Human | P09411 Mouse | P16617 Rat |
Alternative names: | Cell migration-inducing gene 10 protein Epididymis secretory sperm binding protein Li 68p HEL S 68p MGC117307 MGC8947 MIG10 pgk1 PGK1_HUMAN PGKA Phosphoglycerate kinase 1 Primer recognition protein 2 PRP 2 |
Fig1:
Western blot analysis of PGK1 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 (ET1609-63, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Hela cell lysate Lane 2: MCF-7 cell lysate Lane 3: HepG2 cell lysate |
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Fig2: ICC staining of PGK1 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 (ET1609-63, 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: Flow cytometric analysis of PGK1 was done on Hela cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1609-63, 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). |