Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P, FC, IF-Cell, IF-Tissue |
Clonality: | Monoclonal |
Clone number: | JG33-86 |
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: 63 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Glucose 6 phosphate isomerase aa 1-128 / 558. |
Positive control: | A549 cell lysates, HepG2 cell lysates, LO2, MCF-7, human colon tissue, human prostate tissue, human kidney tissue, A549. |
Subcellular location: | Cytoplasm. Secreted. |
Recommended Dilutions:
WB IF-Cell IF-Tissue IHC-P FC |
1:1,000 1:50-1:200 1:50-1:200 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P06744 Human |
Alternative names: | AMF Aurocrine motility factor Autocrine motility factor DKFZp686C13233 EC 5.3.1.9 G6PI_HUMAN Glucose phosphate isomerase Glucose-6-phosphate isomerase GNPI GPI Gpi1 Hexose monophosphate isomerase Hexosephosphate isomerase Neuroleukin NLK Oxoisomerase PGI PHI Phosphoglucose isomerase Phosphohexomutase Phosphohexose isomerase Phosphosaccharomutase SA 36 SA-36 SA36 |
Fig1:
Western blot analysis of Glucose 6 phosphate isomerase on different lysates with Rabbit anti-Glucose 6 phosphate isomerase antibody (ET7108-01) at 1/1,000 dilution. Lane 1: HAP1-parental cell lysate Lane 2: HAP1-Glucose 6 phosphate isomerase KD cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 63 kDa Observed band size: 54 kDa Exposure time: 20 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 (ET7108-01) at 1/1,000 dilution was used in K1803 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: Western blot analysis of Glucose 6 phosphate isomerase on A549 cell lysates and HepG2 cell lysates using anti-Glucose 6 phosphate isomerase antibody at 1/1,000 dilution. | |
Fig3: ICC staining Glucose 6 phosphate isomerase in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig4: ICC staining Glucose 6 phosphate isomerase in LO2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig5: Immunohistochemical analysis of paraffin-embedded human prostate tissue using anti-Glucose 6 phosphate isomerase antibody. Counter stained with hematoxylin. | |
Fig6: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-Glucose 6 phosphate isomerase antibody. Counter stained with hematoxylin. | |
Fig7: Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-Glucose 6 phosphate isomerase antibody. Counter stained with hematoxylin. | |
Fig8: Flow cytometric analysis of A549 cells with Glucose 6 phosphate isomerase antibody at 1/100 dilution (purple) compared with an unlabelled control (cells without incubation with primary antibody; yellow).Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody. |