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- 文献和实验
- 技术资料
- 供应商:
BD Pharmingen
- 靶点:
SSEA-3
- 级别:
RUO
- 克隆性:
单克隆
- 抗体英文名:
SSEA-3 Antibody
- 抗体名:
SSEA-3
- 标记物:
PE
- 宿主:
Rat
- 免疫原:
Mouse Embryos
- 亚型:
Rat F344, also known as Fischer, CDF IgM
- 形态:
液体
- 应用范围:
Flow Cytometry (FCM)
- 保存条件:
2-8℃避光保存
- 规格:
25 Tests
产品概述
SSEA-3 PE MC-631 25Tst 为 BD Pharmingen 品牌流式抗体,货号 560879,靶向 SSEA-3,荧光标记 PE,克隆 MC-631 (also known as MC631) (RUO),规格 25 Tests。适用于 Flow cytometry (Routinely Tested) 检测,仅供科研使用(RUO)。
靶点与抗体说明
The MC-631 monoclonal antibody reacts with S tage- S pecific E mbryonic A ntigen- 3 (SSEA-3), a carbohydrate epitope on the major ganglioside, but not the neutral glycolipid, of mouse embryos and human teratocarcinoma cells. As its name implies, the expression of SSEA-3 is stage-specific and can be used to characterize embryonic cells and monitor their differentiation. However, its expression pattern differs between human and mouse. In the human, SSEA-3 is found on teratocarcinoma (embryonal carcinoma or EC), embryonic inner cell mass (ICM), embryonic stem (ES) cells, and erythrocytes. As human stem cells undergo differentiation, SSEA-3 expression diminishes. In the mouse, SSEA-3 is found on oocytes, ova, zygotes, early cleavage-stage embryos, early blastocysts, ICM, primitive endoderm, and adult kidneys, but not on EC or ES cells.
核心参数
| 货号 | 560879 |
| 品牌 | BD Pharmingen |
| 克隆号 | 克隆 MC-631 (also known as MC631) (RUO) |
| 宿主 | Rat |
| 同种型 | Rat F344, also known as Fischer, CDF IgM |
| 荧光标记 | PE |
| 抗原 / 靶点 | SSEA-3 |
| 验证应用 | Flow cytometry (Routinely Tested) |
| 推荐用量 | 20 µl |
| 免疫原 | Mouse Embryos |
| 规格 | 25 Tests |
| 存储缓冲液 | Aqueous buffered solution containing BSA, protein stabilizer, and ≤0.09% sodium azide. |
荧光染料信息
PE R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye. 格式:PE最多激发源:496 nm, 566 nm最多发射源:576 nm
保存与运输
建议 2-8℃ 避光保存,请勿冷冻,避免反复冻融。 存储缓冲液:Aqueous buffered solution containing BSA, protein stabilizer, and ≤0.09% sodium azide.
参考文献
Draper JS, Pigott C, Thomson JA, Andrews PW. Surface antigens of human embryonic stem cells: changes upon differentiation in culture. J Anat. 2002; 200:249-258. (Clone-specific: Flow cytometry). Henderson JK, Draper JS, Baillie HS, et al. Preimplantation human embryos and embryonic stem cells show comparable expression of stage-specific embryonic antigens. Stem Cells. 2002; 20:329-337. (Clone-specific: Flow cytometry, Immunocytochemistry (cytospins)). Kannagi R, Cochran NA, Ishigami F, et al. Stage-specific embryonic antigens (SSEA-3 and -4) are epitopes of a unique globo-series ganglioside isolated from human teratocarcinoma cells. EMBO J. 1983; 2(12):2355-2361. (Clone-specific: Immunofluorescence). Shevinsky LH, Knowles BB, Damjanov I, Solter D. Monoclonal antibody to murine embryos defines a stage-specific embryonic antigen expressed on mouse embryos and human teratocarcinoma cells. Cell. 1982; 30:697-705. (Immunogen: Cytotoxicity, Immunofluorescence, Immunoprecipitation, Radioimmunoassay). Son YS, Park JH, Kang YK, et al. Heat shock 70-kDa protein 8 isoform 1 is expressed on the surface of human embryonic stem cells and downregulated upon differentiation. Stem Cells. 2005; 23:1502-1513. (Clone-specific: Flow cytometry, Immunocytochemistry (cytospins)). Thomson JA, Itskovitz-Eldor J, Shapiro SS, et al. Embryonic stem cell lines derived from human blastocysts. Science. 1998; 282:1145-1147. (Clone-specific: Immunocytochemistry (cytospins)).
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文献和实验Western Blotting with Horseradish Pe
) is now ready for loading onto your gel. For Protein Concentration Determination of Whole Tissue 1.Rapidly homogenize every 0.25g tissue in 3.5ml of boiling lysis buffer (1% SDS, 1.0mM sodium ortho-vanadate, 10mM Tris pH 7.4). 2.Microwave for 10–15 seconds
T-cell dependent antigen specific in situ staining (Pe)
if you have them). Let them dry approx 1 hour in a dry atmosphere at RT. Antibodies (anti-Pe) in the sections degrade more rapidly than tissue antigens. Proceed with staining within 24 hours or freeze the slides. Antigen-specific staining: (Pe staining of Pe
TCA CAA CTT TAT TGC TGG 3' Length: 21-mer 5' 708 Tm: 64.6 °C (salt 1000.0 mM; oligo 100.0 pM) deltaG (25 °C): -38.8 kcal/mol Degeneracy: 1 P.E.#: 6/410 1/E: 5.06 nmol/A260 33.0 μg/A260 Z23168:948L21 Lower Primer 5' AGC CAT TTT CAA AGC CTC
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