Human Integrin alpha 5/CD49e Antibody Summary
Phe42-Tyr995
Accession # P08648
*Small pack size (-SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
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Detection of Human Integrin a5/CD49e by Western Blot. Western blot shows lysates of K562 human chronic myelogenous leukemia cell line. PVDF Membrane was probed with 1 µg/mL of Goat Anti-Human Integrin a5/CD49e Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1864) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF019). A specific band was detected for Integrin a5/CD49e at approximately 135 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8.
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Detection of Human Integrin alpha 5/CD49e by Simple WesternTM. Simple Western shows lysates of Exosome Standards (U87 MG) (NBP2-49844), Exosome Standards (PC‑3) (NBP2-49856) and Jurkat human acute T cell leukemia cell line, loaded at 0.5 mg/ml. A specific band was detected for Integrin alpha 5/CD49e at approximately 165 kDa (as indicated) using 20 µg/mL of Goat Anti-Human Integrin alpha 5/CD49e Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1864). This experiment was conducted under reducing conditions and using the 12-230kDa separation system.
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Detection of Human Integrin alpha 5/CD49e by Simple WesternTM. Simple Western lane view shows lysates of K562 human chronic myelogenous leukemia cell line, loaded at 0.2 mg/mL. A specific band was detected for Integrin alpha 5/CD49e at approximately 165 kDa (as indicated) using 50 µg/mL of Goat Anti-Human Integrin alpha 5/CD49e Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1864). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.
Reconstitution Calculator
Preparation and 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.
Background: Integrin alpha 5/CD49e
The alpha 5 subunit, also known as CD49e and VLA-5 alpha subunit, forms a heterodimer with the Integrin beta 1 subunit (CD29). Integrin alpha 5 beta 1 is a receptor for fibronectin and neural adhesion molecule L1.
Product Datasheets
Citations for Human Integrin alpha 5/CD49e Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 5
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Induction of cyclophilin A by influenza A virus infection facilitates group A Streptococcus coinfection
Authors: X Bai, W Yang, X Luan, H Li, H Li, D Tian, W Fan, J Li, B Wang, W Liu, L Sun
Cell Reports, 2021-05-18;35(7):109159.
Species: Human
Sample Types: Whole Cells
Applications: Co-Immunoprecipitation, ICC -
Preparation of single- and double-oligonucleotide antibody conjugates and their application for protein analytics
Authors: J Wiener, D Kokotek, S Rosowski, H Lickert, M Meier
Sci Rep, 2020-01-29;10(1):1457.
Species: Mouse
Sample Types: Cell Culture Lysates
Applications: ELISA Capture -
Macrophage-secreted factors promote a profibrotic phenotype in human preadipocytes.
Authors: Keophiphath M, Achard V, Henegar C, Rouault C, Clement K, Lacasa D
Mol. Endocrinol., 2008-10-22;23(1):11-24.
Species: Human
Sample Types: Whole Cells
Applications: Neutralization -
IFATS collection: Combinatorial peptides identify alpha5beta1 integrin as a receptor for the matricellular protein SPARC on adipose stromal cells.
Authors: Nie J, Chang B, Traktuev DO, Sun J, March K, Chan L, Sage EH, Pasqualini R, Arap W, Kolonin MG
Stem Cells, 2008-06-26;26(10):2735-45.
Species: Human
Sample Types: Proteins
Applications: Western Blot -
Gene expression profiling of extracellular matrix as an effector of human hepatocyte phenotype in primary cell culture.
Authors: Page JL, Johnson MC, Olsavsky KM
Toxicol. Sci., 2007-02-27;97(2):384-97.
Species: Human
Sample Types: Cell Lysates
Applications: Western Blot
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