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℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 55 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human KLF4 aa 406-458. |
Positive control: | 293 cell lysate, F9 cell lysate, human colon tissue. |
Subcellular location: | Nucleus. |
Recommended Dilutions:
WB IHC-P FC |
1:500 1:200-1:1,500 1:100 |
Uniprot #: | SwissProt: O43474 Human | Q60793 Mouse |
Alternative names: | Endothelial Kruppel like zinc finger protein Epithelial zinc finger protein EZF EZF GKLF gut Kruppel-like factor Gut-enriched krueppel-like factor KLF KLF4 KLF4_HUMAN Krueppel-like factor 4 Kruppel like factor 4 (Epithelial zinc finger protein EZF) (Gut enriched Krueppel like factor) Kruppel like factor 4 (gut) |
Fig1: Western blot analysis on 293 (1) and F9 (2) cell lysates using anti-KLF4 rabbit polyclonal antibodies. | |
Fig2:
Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-KLF4 antibody (R1308-1) at 1/1,500 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (R1308-1) at 1/1,500 dilution for 1 hour 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. |
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Fig3:
Immunohistochemical analysis of paraffin-embedded human skin tissue with Rabbit anti-KLF4 antibody (R1308-1) at 1/1,500 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (R1308-1) at 1/1,500 dilution for 1 hour 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. |