產(chǎn)品編號 | bs-20810R-Cy5 |
英文名稱 | Rabbit Anti-Perforin/Cy5 Conjugated antibody |
中文名稱 | Cy5標記的穿孔素抗體 |
別 名 | Cytolysin; FLH2; HPLH2; Lymphocyte pore forming protein; Lymphocyte pore-forming protein; MGC65093; P1; PERF_HUMAN; PERF_MOUSE; Perforin 1; Perforin 1 precursor; Perforin 1 preforming protein; Perforin-1; PFP; PGFL; PIGF; PIGF-2; PLGF; Pore forming protein; PRF 1; PRF1; SHGC-10760. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領域 | 細胞生物 淋巴細胞 t-淋巴細胞 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | Mouse, (predicted: Rat, ) |
產(chǎn)品應用 | ICC=1:50-200 IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 60kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from mouse Perforin |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
儲 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存條件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
產(chǎn)品介紹 |
background: The protein encoded by this gene has structural and functional similarities to complement component 9 (C9). Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells. This protein is one of the main cytolytic proteins of cytolytic granules, and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis. Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]. Function: Plays a key role in secretory granule-dependent cell death, and in defense against virus-infected or neoplastic cells. Plays an important role in killing other cells that are recognized as non-self by the immune system, e.g. in transplant rejection or some forms of autoimmune disease. Can insert into the membrane of target cells in its calcium-bound form, oligomerize and form large pores. Promotes cytolysis and apoptosis of target cells by facilitating the uptake of cytotoxic granzymes. Subunit: Monomer, as sobluble protein. Homooligomer. Oligomerization is required for pore formation. Subcellular Location: Cytoplasmic granule lumen. Secreted. Cell membrane. Endosome lumen. Stored in cytoplasmic granules of cytolytic T-lymphocytes and secreted into the cleft between T-lymphocyte and target cell. Inserts into the cell membrane of target cells and forms pores. Membrane insertion and pore formation requires a major conformation change. May be taken up via endocytosis involving clathrin-coated vesicles and accumulate in a first time in large early endosomes. Post-translational modifications: N-glycosylated. DISEASE: Defects in PRF1 are the cause of hemophagocytic lymphohistiocytosis familial type 2 (FHL2) [MIM:603553]; also known as HPLH2. Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous, rare autosomal recessive disorder. It is characterized by immune dysregulation with hypercytokinemia and defective natural killer cell function. The clinical features of the disease include fever, hepatosplenomegaly, cytopenia, hypertriglyceridemia, hypofibrinogenemia, and neurological abnormalities ranging from irritability and hypotonia to seizures, cranial nerve deficits, and ataxia. Hemophagocytosis is a prominent feature of the disease, and a non-malignant infiltration of macrophages and activated T lymphocytes in lymph nodes, spleen, and other organs is also found. Similarity: Belongs to the complement C6/C7/C8/C9 family. Contains 1 C2 domain. Contains 1 EGF-like domain. Contains 1 MACPF domain. Database links: Entrez Gene: 5551 Human Entrez Gene: 18646 Mouse Omim: 170280 Human SwissProt: P14222 Human SwissProt: P10820 Mouse Unigene: 2200 Human Unigene: 240313 Mouse Unigene: 11206 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
1、抗體溶解方法 | |
2、抗體修復方式 | |
3、常用試劑的配制 | |
4、免疫組化操作步驟 | |
5、免疫組化問題解答 | |
6、Western Blotting 操作步驟 | |
7、Western Blotting 問題解答 | |
8、關于肽鏈的設計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 熟妇少妇任你躁91 | 狠狠色7777久夜色 | 少妇浓毛性XXXX法国 | ..少妇泬出白浆狠狠躁日本动漫 | 亚洲精品国产精品园自产A片动漫 | 操逼不卡18禁网站 | 中文字幕av一区二区 | 波多野结衣无码视频在线观看 | 国产黄色视频在线免费观看 | 导管无码毛片av在线 | 色婷婷亚洲精品久久精品无码 | 天天爽日日澡AAAA片 | 性感女性黄色免费观看视频网站 | 午夜理理伦一级A片 | 精品动漫中文子幕三区 | 三级在线观看午夜福利 | 日韩精品一区二区无码 | 黄色激情视频在线观看 | 亚洲AV色香蕉一区二区三区老师 | 国産精品久久久久久久 | 久久久久久久久久久网站 | 高清国产一区二区三区 | 色欲久久久久国产一级 | 精品国产乱码久久久久久1区2区-亚洲 | 白丝校花 扒腿自慰网站 | 东京香蕉东京热一道本DVD | 亚洲AV无码久久精品国产一区 | 91精品国产aⅴ一区二区 | 在线免费电影中文字幕av | 午夜视频在线观看国产 | ,四川少妇搡BBBB搡BBBB | 一区二区在线观看视频 | 18禁在线免费观看av | 东北免费黄色电影网站 | 无码人妻一区二区三区免费京洛会 | 国产日韩精品一区二区 | 日韩无码精品一区二区 | 亚洲国产精品无码久久久 | 国产传媒无码视频免费 | 欧美一级婬片A片免费软件 国产性猛交 XX 乱照片 |