TNF-R1 Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application ![]()
| WB, IHC, IP, ICC |
---|---|
Primary Accession | P19438 |
Other Accession | P19438 |
Host | Rabbit |
Reactivity | Human, Mouse, Rat, Rabbit, Monkey, Bovine, Dog |
Clonality | Polyclonal |
Description | Rabbit Anti-Mouse TNF-R1 Polyclonal |
Target/Specificity | Detects ~55kDa. |
Other Names | Tumor necrosis factor receptor 1 Antibody, TNFR-1 Antibody, TNFRSF1A Antibody, TNFAR Antibody, TNFR1 Antibody |
Immunogen | Peptide corresponding to AA 20-43 of the mouse TNF-R1 sequence, identical to rat and human over those residues |
Purification | Peptide Affinity Purified |
Storage | -20ºC |
Storage Buffer | PBS pH7.4, 50% glycerol, 0.09% sodium azide |
Shipping Temperature | Blue Ice or 4ºC |
Certificate of Analysis | 1 µg/ml of SPC-170 was sufficient for detection of TNFR1 in 20 µg of Hela lysate by colorimetric immunoblot analysis using Goat anti-rabbit IgG:HRP as the secondary antibody. |
Cellular Localization | Cell Membrane | Golgi Apparatus | Golgi Apparatus Membrane |
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Provided below are standard protocols that you may find useful for product applications.
Background
The Tumor Necrosis Factor Receptor (TNFR) also known as Cluster of differentiation (CD120) is a protein that belongs to the (TNF)/ (TNFR) superfamily. TNF interacts with two distinct receptors TNFR1 and TNFR2. These receptors share no homology on their cytoplasmic sequences(1,3).TNFR1 also known as p55/p60 is a high affinity receptor for TNF-α. The TNFR1 has an extracellular domain with variable numbers of cysteine-rich repeats. The functional properties of TNFR1 are targets in new therapies for osteoporosis, chronic inflammatory and autoimmune diseases (1, 2). The TNF-α/TNFR1 receptor complex is responsible for the recruitment and the subsequent activation of the caspase (aspartate-specific cysteine proteases) that regulate apoptosis.
References
1. Kontermann R.E., et al. (2008) J Immunother. 31(3):225-34.
2. Hehlgans T. and Pfeffer K. (2005) Immunology. 115(1):1-20.
3. Al-Lamki S., et al. (2005) The Faseb Journal. 19:1638-1645.
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