Serpin A1 is the archetypal member of the Serpin superfamily of the serine protease inhibitors (1). As one of the most abundant proteinase inhibitors in the circulation, it is synthesized in the liver and secreted into the bloodstream with the major function to protect tissues against neutrophil elastase. A severe Serpin A1 deficiency leads to several clinical complications such as pulmonary emphysema, juvenile hepatitis, cirrhosis, and hepatocellular carcinoma (2). The deficiency is caused by point mutations in naturally occurring Serpin A1 variants (over 70 are known). For example, the Z variant (Glu342 to Lys) forms intracellular inclusion bodies, is not secreted, and leads to a severe Serpin A1 deficiency (3).
Human Serpin A1/ alpha 1‑Antitrypsin Antibody
R&D Systems | Catalog # MAB1268
Key Product Details
Validated by
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Glu25-Lys418
Accession # P01009
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human Serpin A1/ alpha 1‑Antitrypsin Antibody
Western Blot Shows Serpin A1/ alpha 1‑Antitrypsin Specificity Using Knockout Cell Line.
Western blot shows lysates of HepG2 human hepatocellular carcinoma parental cell line and Serpin A1/ alpha 1‑Antitrypsin knockout HepG2 cell line (KO). Nitrocellulose membrane was probed with Mouse Anti-Human Serpin A1/ alpha 1‑Antitrypsin Monoclonal Antibody (Catalog # MAB1268) followed by HRP-conjugated secondary antibody. A specific band was detected for Serpin A1/ alpha 1‑Antitrypsin at approximately 46.7 kDa (as indicated) in the parental HepG2 cell line, but is not detectable in knockout HepG2 cell line. Primary antibody dilution used: 1 ug/ml. The Ponceau stained transfer of the blot is shown. This experiment was conducted under reducing conditions. Image, protocol, and testing courtesy of YCharOS Inc. See ycharos.com for additional details.Detection of Serpin A1/ alpha 1‑Antitrypsin by Immunoprecipitation.
HepG2 human hepatocellular carcinoma cell line lysates were prepared and immunoprecipitation was performed using 2.0 µg of Mouse Anti-Human Serpin A1/ alpha 1‑Antitrypsin Monoclonal Antibody (Catalog # MAB1268) pre-coupled to Dynabeads Protein G. Immunoprecipitated Serpin A1/ alpha 1‑Antitrypsin was detected in Western Blot with a rabbit anti-Serpin A1 used at 1/5000. The Ponceau stained transfer of the blot is shown. SM=4% starting material; UB=4% unbound fraction; IP=immunoprecipitate; HC=antibody heavy chain. Image, protocol and testing courtesy of YCharOS Inc. (ycharos.com).Detection of Human Serpin A1/ alpha 1‑Antitrypsin by Western Blot.
Western blot shows human plasma and lysates of human lung tissue and human kidney tissue. PVDF membrane was probed with 1 µg/mL of Mouse Anti-Human Serpin A1/a1-Antitrypsin Monoclonal Antibody (Catalog # MAB1268) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (HAF018). Specific bands were detected for Serpin A1/a1-Antitrypsin at approximately 50-60 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Serpin A1/ alpha 1‑Antitrypsin in HepG2 Human Cell Line.
Serpin A1/a1-Antitrypsin was detected in immersion fixed HepG2 human hepatocellular carcinoma cell line using Mouse Anti-Human Serpin A1/ a1-Antitrypsin Monoclonal Antibody (Catalog # MAB1268) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; NL007) and counter-stained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
Detection of Human Serpin A1/ alpha 1‑Antitrypsin by Simple WesternTM.
Simple Western lane view shows lysates of human plasma, loaded at 0.2 mg/mL. A specific band was detected for Serpin A1/ alpha 1‑Antitrypsin at approximately 65 kDa (as indicated) using 10 µg/mL of Mouse Anti-Human Serpin A1/ alpha 1‑Antitrypsin Monoclonal Antibody (Catalog # MAB1268). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.Detection of Serpin A1/ alpha 1‑Antitrypsin in Human Prostate.
Serpin A1/ alpha 1‑Antitrypsin was detected in immersion fixed paraffin-embedded sections of Human Prostate using Mouse Anti-Human Serpin A1/ alpha 1‑Antitrypsin Monoclonal Antibody (Catalog # MAB1268) at 5 µg/mL for 1 hour at room temperature followed by incubation with the Anti-Mouse IgG VisUCyte™ HRP Polymer Antibody (Catalog # VC001). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using VisUCyte Antigen Retrieval Reagent-Basic (Catalog # VCTS021). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm in epithelial cells. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents.
Applications for Human Serpin A1/ alpha 1‑Antitrypsin Antibody
Immunocytochemistry
Sample: Immersion fixed HepG2 human hepatocellular carcinoma cell line
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of Human Prostate
Immunoprecipitation
Sample: Conditioned cell culture medium spiked with Recombinant Human Serpin A1/ alpha 1-Antitrypsin (Catalog # 1268-PI), see our available Western blot detection antibodies
Simple Western
Sample: Human plasma
Western Blot
Sample: Human plasma, human lung tissue, and human kidney tissue
Reviewed Applications
Read 5 reviews rated 4.6 using MAB1268 in the following applications:
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.5 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: Serpin A1/alpha 1-Antitrypsin
References
- Silverman, G.A. et al. (2001) J. Biol. Chem. 276:33293.
- Barbour, K.W. et al. (2002) Genomics 80:515.
- Lomas, D.A. et al. (2002) Biochem. Soc. Trans. 30:89.
Alternate Names
Entrez Gene IDs
Gene Symbol
UniProt
Additional Serpin A1/alpha 1-Antitrypsin Products
Product Documents for Human Serpin A1/ alpha 1‑Antitrypsin Antibody
Product Specific Notices for Human Serpin A1/ alpha 1‑Antitrypsin Antibody
For research use only
Related Research Areas
Citations for Human Serpin A1/ alpha 1‑Antitrypsin Antibody
Customer Reviews for Human Serpin A1/ alpha 1‑Antitrypsin Antibody (5)
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Customer Images
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Application: Immunocytochemistry/ImmunofluorescenceSample Tested: NeuronsSpecies: HumanVerified Customer | Posted 10/26/2021
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Application: ELISASample Tested: SeraSpecies: HumanVerified Customer | Posted 12/05/2017
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Application: Western BlotSample Tested: Purified proteinSpecies: HumanVerified Customer | Posted 05/12/2017
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Application: ImmunoprecipitationSample Tested: Human serumSpecies: HumanVerified Customer | Posted 03/03/2017A1AT Std, Human A1AT standard protein (2μg); Human Serum, A1AT protein purified from 10μl human serum using antibody (MAB 1268).
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Application: ELISASample Tested: Cell LysatesSpecies: HumanVerified Customer | Posted 04/26/2016
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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
- 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
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Immunoprecipitation Protocol
- 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 Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- 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 ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- 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
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- 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