Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IF-Tissue, IHC-P, IP |
Clonality: | Monoclonal |
Clone number: | SR46-05 |
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: | Predicted band size: 148 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Collagen XVII aa 1313-1420 / 1497. |
Positive control: | A431 cell lysate, mouse skin tissue lysate, rat skin tissue lysate, HUVEC, human skin tissue, mouse skin tissue, rat skin tissue. |
Subcellular location: | Cell junction, Membrane, Secreted |
Recommended Dilutions:
WB IF-Cell IF-Tissue IHC-P IP |
1:1,000-1:5,000 1:50 1:50 1:50-1:200 Use at an assay dependent concentration. |
Uniprot #: | SwissProt: Q9UMD9 Human | Q07563 Mouse Unigene: 40392 Rat |
Alternative names: | 180 kDa bullous pemphigoid antigen 2 Alpha 1 type XVII collagen BA16H23.2 BP 180 BP180 BPA 2 BPAG 2 BPAG2 Bullous pemphigoid antigen 2 COL17A1 Collagen 17 Collagen alpha 1 XVII chain Collagen alpha 1(XVII) chain Collagen alpha1 XVII chain Collagen type XVII alpha 1 Collagen XVII alpha 1 polypeptide CollagenXVII Epidermolysis bullosa junctional localisata variant FLJ60881 KIAA0204 LAD 1 LAD1 |
Fig1:
Western blot analysis of Collagen XVII on different lysates with Rabbit anti-Collagen XVII antibody (ET1602-14) at 1/5,000 dilution. Lane 1: A431 cell lysate (15 µg/Lane) Lane 2: Mouse skin tissue lysate (20 µg/Lane) Lane 3: Rat skin tissue lysate (20 µg/Lane) Predicted band size: 148 kDa Observed band size: 130、180 kDa Exposure time: 40 seconds; ECL: K1802; 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 (ET1602-14) at 1/5,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. 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: ICC staining of Collagen XVII in HUVEC 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 (ET1602-14, 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:
Immunohistochemical analysis of paraffin-embedded human skin tissue with Rabbit anti-Collagen XVII antibody (ET1602-14) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (ET1602-14) at 1/200 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. |
Fig4:
Immunohistochemical analysis of paraffin-embedded mouse skin tissue with Rabbit anti-Collagen XVII antibody (ET1602-14) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (ET1602-14) at 1/200 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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Fig5:
Immunohistochemical analysis of paraffin-embedded rat skin tissue with Rabbit anti-Collagen XVII antibody (ET1602-14) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (ET1602-14) at 1/200 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. |