Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P, FC |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 36 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein corresponding to N-terminal Human GAL4. |
Positive control: | WB: Human small intestine tissue lysate, mouse colon tissue lysate. IHC: Rat large intestine tissue, human appendix tissue, mouse colon tissue. FC: SHSY5Y cell. |
Subcellular location: | Cytosol. |
Recommended Dilutions:
WB IHC-P FC |
1:500-1:1,000 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P56470 Human | Q8K419 Mouse | P38552 Rat |
Alternative names: | Antigen NY CO 27 Antigen NY-CO-27 Antigen NYCO27 GAL 4 Gal-4 GAL4 Galectin 4 Galectin-4 Galectin4 Homo sapiens galectin4 mRNA complete cds L 36 lactose binding protein L-36 lactose-binding protein L36 lactose binding protein L36LBP Lactose binding lectin 4 Lactose-binding lectin 4 Lectin galactoside binding soluble 4 LEG4_HUMAN LGALS4 |
Fig1:
Western blot analysis of GAL4 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 (ER1902-63, 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: Human small intestine tissue lysate Lane 2: Mouse colon tissue lysate |
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Fig2: Immunohistochemical analysis of paraffin-embedded rat large intestine tissue using anti-GAL4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ER1902-63, 1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human appendix tissue using anti-GAL4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ER1902-63, 1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. | |
Fig4: Immunohistochemical analysis of paraffin-embedded mouse colon tissue using anti-GAL4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ER1902-63, 1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
Fig5: Flow cytometric analysis of GAL4 was done on SHSY5Y cells. The cells were fixed, permeabilized and stained with the primary antibody (ER1902-63, 1/100) (purple). 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 1/500 dilution for 30 minutes. Unlabelled sample was used as a control (cells without incubation with primary antibody; yellow). |