强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
少妇搡BBBB搡BBB搡失恋,亚洲一區二區三区久久久成人動漫,一区二区中文字幕
首頁(yè) > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Perforin Rabbit pAb (bs-20270R)  
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)

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

Entrez Gene: 50669 Rat

Omim: 170280 Human

SwissProt: P14222 Human

SwissProt: P10820 Mouse

SwissProt: P35763 Rat

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.
版權(quán)所有 2004-2026 www.nmgps.com 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
乱婬寡妇一区二区三区 | 精品夜夜澡人妻无码AV蜜桃 | 日本丰满脂肪人人爱视频在线观看50路 | 一区二区免费视频 | 亚洲国产精品视频17c | 无码粉嫩极品尤物在线综合 | 天天干天天射天天操天天日 | 女人高潮一级A片潘金莲 | 91亚洲国产熟妇无码一区二 | 精品乱码一区内射人妻无码 | 九九水密桃亚洲AV无码精 | 91海角社区熟女人妻3p | 免费A片是视频芊芊视频 | 国产BBB搡BBB爽爽爽 | 懂色精品人妻一区二区三区雌奴 | 岳胥乱一区二区三区视频 | 91人妻人人做人碰人人爽九色-百度 | 亚洲一区二区五十路激情中出自拍 | 中文字幕-区二区三区四区视频 | 少妇搡BBBB搡BBB搡毛片 | av网站免费在线观看 | HEYZO高无码国产精品一本蓝牛 | 人人妻人人爽人人添夜夜 | 国产一级a毛一级a看高清视视频 | 天天鲁一鲁摸一摸爽一爽 | 无码人妻视频一区二区 | 亚洲综合激情五月久久 | 81人妻精品无码视频 | 少妇搡BBBB搡BBBB毛多多 | 黄色网址成人在线观看 | 黑丝美女高潮喷水免费网站 | 熟女 人妻蜜臀av一区二区三区 | 又粗又深又猛又爽无遮挡 | 一级毛片中文字幕免费的 | 欧美熟妇另类久久久久久牛牛影视 | 精品黑料一区二区三区 | 欧美成人精品欧美一级私黄 | 最好的2019中文大全在线观看 | 国产精品一区二区五区 | 又粗又深又猛又爽无遮挡 | 国产一级毛片内射年月直播 |