Anti-LAMP1 antibody - Lysosome Marker

6 product images

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMP1 antibody - Lysosome Marker (ab24170)

  IHC image of LAMP1 staining in a section of formalin-fixed paraffin-embedded normal human kidney* performed on a Leica BOND^TM system using the standard protocol B. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20mins. The section was then incubated with ab24170, 1ug/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.
  

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre

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  This image is courtesy of a customer review submitted by Mr Carl Hobbs

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMP1 antibody - Lysosome Marker (ab24170)

  ab24170 staining LAMP1 in human kidney tissue sections. Staining correlates with lysosomal specificity, particularly in the proximal convoluted tubules where lysosomes are enriched. Formalin/PFA-fixed human kidney tissue sections were incubated with ab24170 (1/200) for 2 hours. Antigen retrieval was performed by heat induction in citrate buffer pH 6. Please see accompanying abreview for additional information.

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  Western blot - Anti-LAMP1 antibody - Lysosome Marker (ab24170)

  This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% Milk before being incubated with ab24170 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.
  

  Abcam recommends using milk as the blocking agent. Abcam welcomes customer feedback and would appreciate any comments regarding this product and the data presented above.

  All lanes: Western blot - Anti-LAMP1 antibody - Lysosome Marker (ab24170) at 1 µg/mL

  Lane 1: Jurkat (Human) Whole Cell Lysate at 10 µg

  Lane 2: HEK293 (Human) Whole Cell Lysate at 10 µg

  Secondary

  All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed at 1/50000 dilution

  Developed using the ECL technique.

  Performed under reducing conditions.

  Predicted band size: 45 kDa

  Observed band size: 120 kDa, 20 kDa

  Exposure time: 8min

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  Western blot - Anti-LAMP1 antibody - Lysosome Marker (ab24170)

  All lanes: Western blot - Anti-LAMP1 antibody - Lysosome Marker (ab24170) at 1 µg/mL

  Lane 1: Jurkat (Human T cell lymphoblast-like cell line) Whole Cell Lysate at 10 µg

  Lane 2: A431 (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

  Lane 3: HEK293 Human embryonic kidney cell line Whole Cell Lysate at 10 µg

  Lane 4: MCF7 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 10 µg

  Secondary

  All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed at 1/3000 dilution

  Performed under reducing conditions.

  Predicted band size: 45 kDa

  Observed band size: 120 kDa, 23 kDa, 35 kDa, 45 kDa

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  This image is courtesy of a customer review submitted by Dr. Martin Broadstock (King's College London, United Kingdom)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMP1 antibody - Lysosome Marker (ab24170)

  IHC-P image of LAMP1 staining on human Cortex sections using ab24170 (1:400). The sections were deparaffinized and subjected to heat mediated antigen retreival using citric acid. The sections were then permeabilized using 0.05% Tween-20 and blocking was performed using 3% BSA for 1 hour at 21°C. The primary antibody ab24170 was diluted using 3% BSA with 0.05% Tween-20 in PBS and incubated with the sections for 18 hours at 4°C. The secondary antibody used was Goat polyclonal to rabbit IgG conjugated to biotin (1:500)

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  This image is courtesy of an anonymous customer review

  Western blot - Anti-LAMP1 antibody - Lysosome Marker (ab24170)

  Blocking Step: 5% Milk for 1 hour at 20°C

  All lanes: Western blot - Anti-LAMP1 antibody - Lysosome Marker (ab24170) at 1/700 dilution

  All lanes: Rat Kidney - whole tissue lysate at 18 µg

  Secondary

  All lanes: An HRP-conjugated Goat anti-rabbit IgG polyclonal at 1/5000 dilution

  Developed using the ECL technique.

  Performed under reducing conditions.

  Predicted band size: 45 kDa

  Observed band size: 120 kDa

  Exposure time: 5min