Human phospho-eIF2 alpha (S52) Antibody (849159)
R&D Systems | Catalog # MAB39971
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Key Product Details
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Label
Antibody Source
Product Specifications
Immunogen
Accession # P05198
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human phospho-eIF2 alpha (S52) Antibody (849159)
Detection of Human Phospho-eIF2 alpha (S52) by Western Blot.
Western blot shows lysates of HeLa human cervical epithelial carcinoma cell line and HEK293T human embryonic kidney cell line untreated (-) or treated (+) with 100nM Calyculin A (Catalog # 1336) and 20 ng/mL Recombinant Human TNF-a (Catalog # 210-TA) for 10 minutes or 20 mJ/cm2 ultraviolet light (UV) followed by a 30 minute recovery. PVDF membrane was probed with 1 µg/mL of Rat Anti-Human Phospho-eIF2a (S52) Monoclonal Antibody (Catalog # MAB39971) followed by HRP-conjugated Anti-Rat IgG Secondary Antibody (Catalog # HAF005). A specific band was detected for Phospho-eIF2a (S52) at approximately 38 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.Detection of Phospho-eIF2 alpha (S52) by Western Blot
Analysis of signal transduction during CHIKV infection in the presence of 50 nM silvestrol. (A) HEK 293T cells were seeded in six-well plates and were infected with CHIKV using an MOI of 1, and 50 nM silvestrol was added where indicated. Cells were treated with IFN alpha for 30 min before harvest if indicated, and Western blot analysis of cell lysates was performed. (−) Untreated cells; (+) treated cells. In lanes 3–6, cells were infected with CHIKV. The CHIKV E2 protein, STAT1, eIF2 alpha, and their phosphorylated proteins were detected with specific antibodies and secondary HRP-coupled antibodies, and the ECL detection system (Amersham, Freiburg). Equal loading of each blot was controlled by detection of beta -actin; and, (B) Uninfected HEK293T cells were treated with IFN alpha for 30 min before harvest and either treated with silvestrol for 16 h or left untreated. Western blot analysis of cell lysates was performed and p-STAT1 and STAT1 were detected. STAT1 served as a loading control. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/30380742), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human phospho-eIF2 alpha (S52) Antibody (849159)
Western Blot
Sample: HeLa human cervical epithelial carcinoma cell line and HEK293T human embryonic kidney cell line treated with Calyculin A and Recombinant Human TNF‑ alpha (Catalog # 210-TA) or ultraviolet light (UV)
Reviewed Applications
Read 1 review rated 5 using MAB39971 in the following applications:
Formulation, Preparation, and Storage
Purification
Reconstitution
Sterile PBS to a final concentration of 0.5 mg/mL. 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: eIF2 alpha
Long Name
Alternate Names
Gene Symbol
UniProt
Additional eIF2 alpha Products
Product Documents for Human phospho-eIF2 alpha (S52) Antibody (849159)
Certificate of Analysis
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Product Specific Notices for Human phospho-eIF2 alpha (S52) Antibody (849159)
For research use only
Related Research Areas
Citations for Human phospho-eIF2 alpha (S52) Antibody (849159)
Customer Reviews for Human phospho-eIF2 alpha (S52) Antibody (849159) (1)
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Cellular Response to Hypoxia Protocols
- R&D Systems Quality Control Western Blot Protocol
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
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