產(chǎn)品編號(hào) | bs-20270R-Gold |
英文名稱 | Rabbit Anti-Perforin/Gold Conjugated antibody |
中文名稱 | 膠體金標(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(10nm 15nm 35nm) |
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) | Human, |
產(chǎn)品應(yīng)用 | IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200
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 | 0.4mg/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(chǔ) 存 液 | 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300. |
保存條件 | Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles. |
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. |
| 中文字幕乱码亚洲精品一区 | 少妇做受XXXXⅩ高潮片直播 | 亚洲AV色香蕉一区二区三区老师 | 熟女五十路欲求不满在线播放 | 高清无码熟妇在线播放 | 欧美性XXX黑人XYX | 97人妻人人揉人人澡人 | 国产亚洲综合一区二区 | 特级毛片片A片AAAAAA | 国产免费人做人爱午夜视频 | 黄色高清无码免费观看 | 国产精品岛国久久久久久 | 色婷婷一区二区三区久久午夜成人 | 免费无码婬片AAAA片上门服务 | 国产精品秘 麻豆人口 | 亚洲色精品三区二区一区 | 一本大道伊人精品无码A色欲 | 日本老熟妇人妻妇毛多多 | 无码人妻精品一区二区蜜桃91 | 精品人人搡人妻人人玩A片 国产免费观看黄色电视网站 | 100国产精品人妻无码 | 五十路09豊满十9肉体 | 一区二区三区无码视频 | 国产白丝护士喷白浆视频 | 四虎8848成人永久视频 | 国产精产国品91在线看 | 日本精品中文字幕人妻 | 国产无人区一区二区三区四区 | 香蕉视频黄色96 | 国产91亚洲精品成人AA片p站 | 亚洲天堂毛片在线观看 | 国产真实亲子伦脏话对白免费影视 | 亚洲+小说+欧美+激情+另类 | 国产小电影在线观看 | 在线观看无码视频 | 国产精品无码粉嫩小泬 | 后人翘臀少妇在线观看 | 工口动画无料影音先锋资源 | 欧美精品在线观看 | 国产无遮挡无黄又爽农村妇女 |