| Isotype | IgG1 (F)/IgG2b (PE) |
| Product Type | Bi-Testª Reagents (FITC/RPE) |
| Units | 50 Tests |
| Host | Mouse |
| Species reactivity | Human |
| Application | Flow Cytometry |
BackgroundCD56, M.W. 150,000, is expressedonapproximately 10-25%ofhuman peripheral blood lymphocytes. CD56 (NKH-1) is expressed on human peripheral blood natural killer cells, representing a pan NK-cell antigen. Expressed on non-MHC-restricted cytotoxic T cells.
Synonyms: CD8 FITC - CD56 PE
Source
Immunogen: CD8=Derived from the hybridization of mouse NS-1 myeloma cells with spleen cells from BALB/c mice immunized with human perherial blood T lymphocytes.CD56=Derived from the hybridization of mouse Sp2/0 myeloma cells with spleen cells from BALB/cF1 mice immunized with KG1a cell line.
Product
Product Form: Bi-Test (FITC/RPE) Reagent
Formulation: Provided as solution in phosphate buffered saline with 0.08% sodium azide and 0.2% carrier protein
Purification Method: Protein A/G Chromatography
Concentration: Titered for flow cytometry
ApplicationsPBMC: Add 10 µl of MAB/10^6 PBMC in 100 µl PBS. Mix gently and incubate for 15 minutes at 2º to 8º C. Wash twice with PBS and analyze or fix with 0.5% v/v ofparaformaldehyde in PBS and analyze. WHOLE BLOOD: Add10 µl of MAB/100 µl of whole blood. Mix gently and incubate for 15minutes at room temperature 20ºC. Lyse the whole blood. Wash once with PBS and analyze or fix with 0.5% v/v of paraformaldehyde in PBS and analyze. See instrument manufacturer’s instructions for Lysed Whole Blood and Immunofluorescence analysiswith a flow cytometer or microscope.
Functional Analysis: Flow Cytometry Staining
StorageProduct should be stored at 4-8ºC. DO NOT FREEZE
Product Stability: Reagents are stable for the period shown on the vial label when stored properly
Shipping Conditions: Room Temperature
CautionThis product is intended FOR RESEARCH USE ONLY, and FOR TESTS IN VITRO, not for use in diagnostic or therapeutic procedures involving humans or animals. It may contain hazardous ingredients. Please refer to the Safety Data Sheets (SDS) for additional information and proper handling procedures. Dispose product remainders according to local regulations.This datasheet is as accurate as reasonably achievable, but Nordic-MUbio accepts no liability for any inaccuracies or omissions in this information.
References1. Evolutionary Conservation of Surface Molecules that Distinguish T Lymphocyte Helper/Inducerand T Cytotoxic/Suppressor Subpopulations in Mouse and Man. Ledbetter,J.A., Evans,R.L., Lipinski,M., Cunningham-Rundles,C., Good,R.A. and Herzenberg,L.A., J. Exp. Med. 153,310, 1981. 2. Circulating Antigen-Specific Suppressor T Cells in a Healthy Woman: Mechanism of Action and Isolation with a Monoclonal Antibody.Engleman,E.G.,Benike,C.J.,and Evans,R.L., Clin. Res. 29, 365a 1981. 3. Induction of Immunoglobulin Secreting Cells in the Allogeneic Mixed Leukocyte Reaction: Regulation by Helper and Suppressor Lymphocyte Subsets in Man.Kotzin,B.L., Benike,C.J. andEngleman,E.G., J. Imm. 127,931,1981.4. CD4 and CD8 molecules can physically associate with the same T-cell receptor.Gallagher,P.F., Fazekas de St. Groth,B., Miller, J.F.A.P., Proc. Nat. Acad. Sci. 1989,86:10044.5. Immunofluorescence Measurement in a Flow Cytometer using Low-Power Helium Neon LaserExcitation.Shapiro, H.M, Glazer, A.N., Christenson, L., Williams, J.M., and Strom, T. B. Cytometry 4,276, 1983. 6. Comparison of Helium Neon and Dye lasers for Excitation of Allophycocyanin.Loken, M.R., Kiej, J.F. and Kelly, K.,A.Cytometry 8, 96, 1987. 7. Generation of Monoclonal Antibodies to a Human Natural Killer Clone. Characterization of Two Natural Killer-Associated Antigens, NKH1 and NKH2, Expressed on Subset of Large Granular Lymphocytes. Hercend, T., Griffin, J.D., Benussan, A., Schmidt, R.E., Edson, M.A., Brennen, A.,Murray, C., Daley, J.F., Schlossman, S.F., and Ritz, J..J. Clin. Invest. 1985 75:932. 8. The relationship of CD16 (Leu-11) and Leu-19 (NKH-1) Antigen Expression on Human Peripheral Blood Nk Cells and Cytotoxic T Lymphocytes. Lanier, L.L., Le, A.M., Civin, C.I., Loken, M.R., and Phillips, J.H.,J. Immunol. 1986 136,4480. 9. A subset of natural killer cells in peripheral blood displays a mature T cell phenotype. Schmidt RE, Murray C, Daley JF, Schlossman SF, and Ritz J,J Ex Med 1986 164: 351-356 10. Phenotypic and functional deficiency of natural killer cells in patients with chronic fatigue syndrome. Caligiuri M, Murray C, Buchwald D, Levine H, Cheney P, Peterson D, Komaroff AL,and Ritz J,J Immunol 1987 139:3306-331911. Hercend T., and Schmidt, R.E., Immunol. Today 9,291,1988.
Protein Reference(s)
Database Name: UniProt
Accession number: P01732, P13591
Safety Datasheet(s) for this product:NM_Sodium Azide/wp-content/uploads/SDS/Antibody SDS with Sodium Azide Noridic-MUbio.pdf
ebiomall.com
>
>
>
>
>
>
>
>
>
>
>
>
抗体都是免疫球蛋白而免疫球蛋白不一定都是抗体。原因是抗体是由浆细胞产生,且能与相应抗原特异性结合发挥免疫功能的球蛋白。而免疫球蛋白是具有抗体活性或化学结构与抗体相似的球蛋白,如骨髓瘤患者血清中异常增高的骨髓瘤蛋白,是由浆细胞瘤产生,其结构与抗体相似,但无免疫功能。因此,免疫球蛋白可看做是化学结构上的概念,抗体则是生物学功能上的概念。
二、保持乐观情绪乐观的态度可以维持人体于一个最佳的状态,尤其是在现今社会,人们面临的压力很大,巨大的心理压力会导致对人体免疫系统有抑制作用的荷尔蒙成分增多,所以容易受到感冒或其它疾病的侵袭。
三、限制饮酒每天饮低度白酒不要超过100毫升,黄酒不要超过250毫升,啤酒不要超过1瓶,因为酒精对人体的每一部分都会产生消极影响。即使喝葡萄酒可以降低胆固醇,也应该限制每天一杯,过量饮用会给血液与心脏等器官造成很大破坏。
四、参加运动专家进行的3项研究指出,每天运动30到45分钟,每周5天,持续12周后,免疫细胞数目会增加,抵抗力也相对增加。运动只要心跳加速即可,晚餐后散步就很适合。
五、补充维生素每天适当补充维生素和矿物质。专家指出,身体抵抗外来侵害的武器,包括干扰素及各类免疫细胞的数量与活力都和维生素与矿物质有关。
六、改善体内生态环境用微生态制剂提高免疫力的研究和使用由来已久。研究表明,以肠道双歧杆菌、乳酸杆菌为代表的有益菌群具有广谱的免疫原性,能刺激负责人体免疫的淋巴细胞分裂繁殖,同时还能调动非特异性免疫系统,去“吃”掉包括病毒、细菌、衣原体等在内的各种可致病的外来微生物,产生多种抗体,提高人体免疫能力。对于健康人来说,不妨“食疗”,多吃些乳酸菌饮料;而健康边缘人群,可以用微生态制剂来调节体内微生态平衡。能提高免疫力的食品
1.灵芝:灵芝可增强人体的免疫力,这是因为灵芝含有抗癌效能的多糖体,此外,还含有丰富的锗元素。锗能加速身体的新陈代谢,延缓细胞的衰老,能通过诱导人体产生干扰素而发挥其抗癌作用;
2.新鲜萝卜:因其含有丰富的干扰素诱导剂而具有免疫作用;
3.人参蜂王浆:能提高机体免疫力及内分泌的调节能力,并含具有防癌作用的蜂乳酸;
4.蘑菇、猴头菇、草菇、黑木耳、银耳、车养、百合等:都有明显增强免疫力的作用;
5.香菇:香菇所含的香菇多糖能增强人体免疫力。展开

