產(chǎn)品編號 | bs-7128R-BF647 |
英文名稱 | Rabbit Anti-Perforin/BF647 Conjugated antibody |
中文名稱 | BF647標(biāo)記的穿孔素抗體 |
別 名 | Cytolysin; FLH2; HPLH2; Lymphocyte pore forming protein; Lymphocyte pore-forming protein; MGC65093; P1; PERF_HUMAN; 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(jià)格 | 100ul/2980元 購買 大包裝/詢價(jià) |
說 明 書 | 100ul |
研究領(lǐng)域 | 細(xì)胞生物 淋巴細(xì)胞 t-淋巴細(xì)胞 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Rat, (predicted: Human, Mouse, Horse, ) |
產(chǎn)品應(yīng)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 | 59kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human 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. |
| 高潮毛片无遮挡免费高清古代的 | 国产电影一区二区三区 | 国产成人无码A片V99 | 孕妇性交久久xxxAV片 | 国产精品视频一区二区三区, | 国产成人精品AA毛片 | 国产亚洲色婷婷久久精品 | 国产一级婬片AAAAA片口述 | 黄色视频在线观看高清无码 | 蜜桃视频污在线免费观看 | 四川少妇BBB凸凸凸BBB按摩 | 色乱一区二区三区四区五匹 | 免费观看黄网站 入口 | 无言一区二区三区无语 | 国产老女人乱婬免费 | 欧美成人午夜无码A片 | 国产成人无码A片V99 | 亚洲一区二区三区在线 | 国产成人久久精品77777综合 | 欧美色图深深插狠狠插 | 亚州成a人无码毛片A片直播平台 | 亚洲美女台湾三级片玖玖 | 麻豆av大片在线观看 | 久久人人爽人人人人片 | 国产99久久久国产精品免费看 | 四川美女一片毛片 | 蜜桃视频一区二区三区 | 日本人成A片在线一区二区 人人添人人澡人人爽人人澡 | 国产精品a久久久久久 | 久久,,,,,。。。。精品 | 国产黄色视频在线观看 | 亚洲中文字幕无码在线观看va6 | 国产一级av免费观看 | 少妇婬片A级毛片贵妇 | 手机在线不卡无码操三八 | .国産黃色視頻免費看 | 成人网站大胸免费看 | 免费毛片全部不收费的 | 乱一色一乱一性一视频 | 无码人妻精品一区二区蜜桃色欲 |