Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Immunocytochemistry [2]
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Validation data
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- Product number
- ALX-804-300-C100 - Provider product page
- Provider
- Enzo Life Sciences
- Proper citation
- Enzo Life Sciences Cat#ALX-804-300-C100, RRID:AB_2052720
- Product name
- TRAIL (human) monoclonal antibody (HS501)
- Antibody type
- Monoclonal
- Antigen
- Recombinant full length protein
- Reactivity
- Human
- Host
- Mouse
- Isotype
- IgG
- Antibody clone number
- HS501
- Vial size
- 100 μg
- Storage
- -80°C
- Handling
- Thaw at +37¡C. Avoid freeze/thaw cycles.
Submitted references TNF-related apoptosis-inducing ligand mediates tumoricidal activity of human monocytes stimulated by Newcastle disease virus.
Washburn B, Weigand MA, Grosse-Wilde A, Janke M, Stahl H, Rieser E, Sprick MR, Schirrmacher V, Walczak H
Journal of immunology (Baltimore, Md. : 1950) 2003 Feb 15;170(4):1814-21
Journal of immunology (Baltimore, Md. : 1950) 2003 Feb 15;170(4):1814-21
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Supportive validation
- Submitted by
- Enzo Life Sciences (provider)
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- Experimental details
- Equal numbers of Jurkat cells treated and untreated with IFNa compared with equal numbers of CV1-EBNA cells transfected with human TRAIL and a control expression plasmid (not encoding hTRAIL) were analyzed by using HS501 (Prod. No. ALX-804-300. Method: Jurkat cells were treated with IFNa [1000 IU/ml] for 8 hours (lane 1) or were left untreated (lane 2), and CV1-EBNA cells were transfected with pcDNA3 expression vector encoding human TRAIL (lane 3), or with human TRAIL-R1 (lane 4). Lysates of equal numbers of cells were analyzed by Western blot with anti-TRAIL HS501 (Prod. No. ALX-804-300). The primary antibody was used at 1µg/ml, followed by horseradish peroxidase-conjugated anti-mouse IgG1 antibody and developed by ECL.
- Submitted by
- Enzo Life Sciences (provider)
- Main image
- Experimental details
- Equal numbers of CV1-EBNA cells transfected with control expression plasmids (negative for human TRAIL) were analyzed and compared to a positive control cell-lysate using HS501. Method: CV1-EBNA cells, either transfected with pcDNA3 expression vector encoding TRAIL-R1 to TRAIL-R4 (lanes 1-4), or with human TRAIL (lane 5) were analyzed with HS501 MAb against TRAIL (Prod. No. ALX-804-300). The primary antibody was used at 1µg/ml, followed by a horseradish peroxidase conjugated anti-mouse IgG1 antibody and developed by ECL.