Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | 26 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within C-terminal human CLIC3 aa 50-236 / 236. |
Positive control: | Human placenta tissue lysate, mouse lung tissue lysate, human lung tissue lysate, rat lung tissue lysates, human esophagus tissue. |
Subcellular location: | Nucleus. |
Recommended Dilutions:
WB IHC-P |
1:500-1:2,000 1:100-1:500 |
Uniprot #: | SwissProt: O95833 Human | Q9D7P7 Mouse | D3ZY91 Rat |
Alternative names: | 2300003G24Rik Chloride intracellular channel 3 Chloride intracellular channel protein 3 MGC109225 OTTHUMP00000022630 |
Fig1:
Western blot analysis of CLIC3 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA500316, 1/500) was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Human placenta tissue lysate Lane 2: Mouse lung tissue lysate Lane 3: Human lung tissue lysate |
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Fig2: Western blot analysis of CLIC3 on rat lung tissue lysate. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA500316, 1/500) was used in 5%NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human esophagus tissue using anti-CLIC3 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) 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 (HA500316, 1/400) 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. |