货号:550320
品牌:BD Pharmingen
规格:100ug
目录价:¥3800.00
市场价格:¥2394.00
会员价格:¥2090.00
金山科研平台,产品价格货期咨询微信:jinshanbio
Contents
with 150 mM NaCl and 0.09% (w/v) sodium azide.
Preparation and Storage
The antibody was purified from tissue culture supernatant by affinity chromatography. The antibody solution should be stored undiluted at 4°C.
Usage
This antibody has been tested by immunofluorescent staining ( 1 µg/million cells) with flow cytometric analysis to assure specificity and reactivity. Since this antigen is expressed at low density on lymphoid cell surfaces, it may be desirable to amplify staining by using a biotinylated second-step antibody, such as goat anti-rat Ig polyclonal antibody (Cat. no. 554050), followed by a "bright" third-step reagent, such as Streptavidin-PE (Cat. no. 554061) or Streptavidin-APC (Cat. no. 554067). In order to obtain a bright staining on LAK (Lymphokine-activated killer) cells, we suggested the use of A-LAK cells (adherent-LAK cells) that had been activated with 3,000 U/ml of recombinant human IL-2 (Cat. no. 554603). Other reported applications include western blot analysis2 and blocking of IL-2/IL-15–activated NK-cell cytotoxicity against mouse fibrosarcoma L929 target cells.1 Immunohistochemical staining of frozen or paraffin-embedded sections is not recommended. Since applications vary, each investigator must determine dilutions appropriate for individual use.
Caution
Sodium azide is a reversible inhibitor of oxidative metabolism; therefore, antibody preparations containing this preservative agent must not be used in cell cultures nor injected into animals. Sodium azide may be removed by washing stained cells or plate-bound antibody or dialyzing soluble antibody in sodium azide-free buffer. Since endotoxin may also affect the results of functional studies, we recommend the NA/LE™ (No Azide/Low Endotoxin) antibody format for in vitro and in vivo use.
Conditions
BD PharMingen will not be responsible for violations or patent infringements which may occur with the use of our products.
- Catalog Number
- 550320
- Brand
- BD Pharmingen™
- Name
- CD253
- Alias
- TRAIL
- Concentration
- 0.5 mg/ml
- Size
- 0.1mg
- RegulatoryStatus
- RUO
- Clone
- N2B2
- Format
- Purified
- Isotype
- IgG2a, κ
- W.B. Positive Control
- none
- Immunogen
- Mouse Trail-transfected 2PK-3 cells
- Strain Host
- F344
- Reactivity
- QC Testing : Mouse
- Applications
-
Flow cytometry | - Routinely Tested |
Western Blot | - Reported |
Clone - References
1. Kayagaki, N., N. Yamaguchi, M. Nakayama, K. Takeda, H. Akiba, H. Tsutsui, H. Okamura, K. Nakanishi, K. Okumura, and H. Yagita. 1999. Expression and function of TNF-related apoptosis-inducing ligand on murine activated NK cells. J. Immunol. 163: 1906 - 1913.2. BD PharMingen. Unpublished results.3. Degli-Esposti, M. 1999. To die or not to die--the quest of the TRAIL receptors. J. Leukoc. Biol. 65: 535 - 542.4. Wu, G.S., T.F. Burns, Y. Zhan, E.S. Alnemri, and W.S. El-Deiry. 1999. Molecular cloning and functional analysis of the mouse homologue of the KILLER/DR5 tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) death receptor. Cancer Res. 59: 2770 - 2775.5. Mariani, S.M., and P.H. Krammer. 1998. Surface expression of TRAIL/Apo-2 ligand in activated mouse T and B cells. Eur. J. Immunol. 28: 1492 - 1498.6. Mariani, S.M., and P.H. Krammer. 1998. Differential regulation of TRAIL and CD95 ligand in transformed cells of the T and B lymphocyte lineage. Eur. J. Immunol. 28: 973 - 982.7. Musgrave, B.L., T. Phu, J.J. Butler, A.P. Makrigiannis, and D.W. Hoskin. 1999. Murine TRAIL (TNF-related apoptosis inducing ligand) expression induced by T cell activation is blocked by rapamycin, cyclosporin A, and inhibitors of phosphatidylinositol 3-kinase, protein kinase C, and protein tyrosine kinases: evidence for TRAIL induction via the T cell receptor signaling pathway. Exp. Cell Res. 252: 96 - 103.
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