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Key Product Details
Species Reactivity
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Label
Antibody Source
Product Specifications
Immunogen
Met1-Asn346
Accession # P04083
Specificity
Clonality
Host
Isotype
Scientific Data Images for Annexin A1 Antibody
Detection of Human/Mouse/Rat Annexin A1 by Western Blot.
Western blot shows lysates of MOLT-4 human acute lymphoblastic leukemia cell line, NIH-3T3 mouse embryonic fibroblast cell line, and L6 rat myoblast cell line. PVDF membrane was probed with 0.2 µg/mL of Goat Anti-Human/Mouse/Rat Annexin A1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3770) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (HAF109). A specific band was detected for Annexin A1 at approximately 35-40 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 2.Detection of Human and Mouse Annexin A1 by Simple WesternTM.
Simple Western shows lysates of Exosome Standards (HT-29) (NBP3-11685), Exosome Standards (U87 MG) (NBP2-49844) and MOLT‑4 human acute lymphoblastic leukemia cell line, loaded at 0.5 mg/ml. A specific band was detected for Annexin A1 at approximately 42 kDa (as indicated) using 10 µg/mL of Goat Anti-Human/Mouse/Rat Annexin A1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3770). This experiment was conducted under reducing conditions and using the 12-230kDa separation system.Annexin A1/Annexin I in Human Breast.
Annexin A1/Annexin I was detected in immersion fixed paraffin-embedded sections of human breast using Goat Anti-Human/Mouse/Rat Annexin A1/Annexin I Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3770) at 10 µg/mL overnight at 4 °C. Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (CTS013). Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; CTS008) and counter-stained with hematoxylin (blue). Specific staining was localized to stromal cells. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Detection of Annexin A1 by Immunohistochemistry
Annexin A1 is coexpressed with S100-A11 in liver metastasis extracellular matrix (ECM) and across other cancer types. A: normalized abundance of annexin A1 and S100-A11 in the quantitative proteomics data set from this study. Each circle indicates a replicate. B and C: coexpression of annexin A1 and S100-A11 in the Tissue Cancer Genome Atlas (TCGA) data set (colorectal adenocarcinoma), as assessed by mRNA (B) and protein (C) levels. Each circle represents a patient. D: coexpression of annexin A1 and S100-A11 in the Cancer Cell Line Encyclopedia data set. Each circle represents a human cancer cell line. ALL, acute lymphoblastic leukemia; AML, acute myelogenous leukemia; CML, chronic myelogenous leukemia; DLBCL, diffuse large B cell lymphoma; NSCLC, nonsmall cell lung carcinoma. A–D: Spearman rank correlation was measured. E: immunostaining for annexin A1 and S100-A11 in the decellularized and cryosectioned ECM from MC38 murine liver metastasis. Negative IgG control staining is shown to the left. Original scale bars, 100 μm. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/31545917), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Annexin A1 Antibody
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of human breast
Simple Western
Sample: Exosome Standards (HT-29) (Catalog # NBP3-11685), Exosome Standards (U87 MG) (Catalog # NBP2-49844), and MOLT-4 human acute lymphoblastic leukemia cell line
Western Blot
Sample: MOLT-4 human acute lymphoblastic leukemia cell line, NIH-3T3 mouse embryonic fibroblast cell line, and L6 rat myoblast cell line
Reviewed Applications
Read 2 reviews rated 4 using AF3770 in the following applications:
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: Annexin A1
Alternate Names
Gene Symbol
UniProt
Additional Annexin A1 Products
Product Documents for Annexin A1 Antibody
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Annexin A1 Antibody
For research use only
Related Research Areas
Citations for Annexin A1 Antibody
Customer Reviews for Annexin A1 Antibody (2)
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Customer Images
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Application: Western BlotSample Tested: liver and Mouse embryonic fibroblastsSpecies: HumanVerified Customer | Posted 06/01/2016Primary ab dilution 1:4000 40 ug protein per lane
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Application: Western BlotSample Tested: See PMID 20618702Species: HumanVerified Customer | Posted 01/08/2015
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars