產(chǎn)品編號(hào) | bs-20270R |
英文名稱 | Perforin Rabbit pAb |
中文名稱 | 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. |
研究領(lǐng)域 | 細(xì)胞生物 淋巴細(xì)胞 t-淋巴細(xì)胞 |
抗體來(lái)源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human |
產(chǎn)品應(yīng)用 | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理論分子量 | 59 kDa |
檢測(cè)分子量 | |
細(xì)胞定位 | 細(xì)胞漿 細(xì)胞膜 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human Perforin: 101-200/555 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
PubMed | PubMed |
產(chǎn)品介紹 |
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. SWISS: P14222 Gene ID: 5551 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 |
產(chǎn)品圖片 |
Paraformaldehyde-fixed, paraffin embedded (human liver carcinoma); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (Perforin) Polyclonal Antibody, Unconjugated (bs-20270R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
|
| 亚洲无码在线网站 | 国产精品秘 入口66mio男同 | 久久黄色视频可看中文无码 | 好爽好硬好深偷拍视频 | 无码人妻精品一区二区蜜桃苍井空 | 久久久久久国产成人a亚洲精品无码 | 17c 在线观看喷潮数学 | 国产精品99朵亚视频免费 | 亚洲最猛黑A片黑人猛交 | 人人妻人人洗澡人人 | 少妇搡BBBB搡BBB搡老女王 | 美女搡BBB又爽又猛又黄www | 精品国产乱码久久久久久蜜柚 | 黄片一区二区三区四区五区六区七区 | 日本一区二区三区久久娇喘 | 哈尔滨熟女白浆91九色 | 国产污污视频在线观看 | 国产69精品久久久久久 | 日韩视频在线观看免费 | 国产自产精品一区二区色欲AV | 日本三色黄A片免费播放 | 人妻人人澡人人添人人爽冫 | 国产日本无码视频韩国网站写真 | 性一交一乱一交A片久久四色 | 蜜桃AV秘一区二区三区 | 免费观看亚洲操逼视频 | A片试看120分钟做受视频红杏 | 国产视频秘 福利姬在线 | 五月天婷亚洲天综合网综合 | 国产精品久久久久久久曹县翰林府 | 熟女一区二区三区 | 国产免费一品二区三区在线播放 | 99热成人精品热久久66 | 国产精品久久久久高潮色老头 | 亚洲精品国产成人综合久久久久久久久 | 国产一级片免费观看 | 波多野结衣国产区42部 | 粉嫩av一区二区白浆 | 亚洲无码电影在线观看 | 亚洲色无色A片一区二区 |