Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JE62-35 |
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: 37 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human Syntaxin 16 aa 50-100/325. |
Positive control: | MCF-7 cell lysate, SK-Br-3 cell lysate, Hela cell lysate, mouse lung tissue lysate, rat testis tissue lysate, rat brain tissue, mouse brain tissue, mouse cerebellum tissue. |
Subcellular location: | Golgi apparatus membrane, Cytoplasm. |
Recommended Dilutions:
WB IHC-P |
1:1,000-1:2,000 1:100-1:500 |
Uniprot #: | SwissProt: O14662 Human | Q8BVI5 Mouse Entrez Gene: 362283 Rat |
Alternative names: | hsyn16 MGC90328 Stx16 STX16_HUMAN Syn16 Syntaxin-16 |
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Fig1:
Western blot analysis of Syntaxin 16 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 (HA720107, 1/500) was used in 5% BSA 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 2: MCF-7 cell lysate Lane 2: SK-Br-3 cell lysate Lane 2: Hela cell lysate Lane 1: Mouse lung tissue lysate Lane 2: Rat testis tissue lysate |
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Fig2: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-Syntaxin 16 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720107, 1/100) 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. |
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Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-Syntaxin 16 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720107, 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. |
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Fig4: Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue using anti-Syntaxin 16 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720107, 1/100) 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. |