超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
伦人伦XXX国产对白,久久人人97超碰com,国产传媒在线视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Munc 13-4/BF647 Conjugated antibody (bs-19103R-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-19103R-BF647
英文名稱 Rabbit Anti-Munc 13-4/BF647 Conjugated antibody
中文名稱 BF647標記的UNC13D蛋白抗體
別    名 FHL 3; FHL3; FLJ00067; HLH 3; HLH3; HPLH 3; HPLH3; Jinx; Munc13 4; Munc13-4; Protein unc 13 homolog D; Protein unc-13 homolog D; UN13D_HUMAN; Unc 13 homolog D; UNC 13D; Unc-13 homolog D (C. elegans); Unc13 homolog D (C elegans); Unc13 homolog D; UNC13, C. elegans, homolog of, D; UNC13D; Unc13h4  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  免疫學  t-淋巴細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rhesus monkey)
產品應用 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 123kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Munc 13-
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.
產品介紹 background:
This gene encodes a protein that is a member of the UNC13 family, containing similar domain structure as other family members but lacking an N-terminal phorbol ester-binding C1 domain present in other Munc13 proteins. The protein appears to play a role in vesicle maturation during exocytosis and is involved in regulation of cytolytic granules secretion. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3, a genetically heterogeneous, rare autosomal recessive disorder. [provided by RefSeq, Jul 2008]

Function:
Plays a role in cytotoxic granule exocytosis in lymphocytes. Required for both granule maturation and granule docking and priming at the immunologic synapse. Regulates assembly of recycling and late endosomal structures, leading to the formation of an endosomal exocytic compartment that fuses with perforin-containing granules at the immunologic synapse and licences them for exocytosis. Regulates Ca(2+)-dependent secretory lysosome exocytosis in mast cells.

Subcellular Location:
Cytoplasm. Membrane. Late endosome. Recycling endosome. Lysosome. Colocalizes with cytotoxic granules at the plasma membrane. Localizes to endosomal exocytic vesicles.

Tissue Specificity:
Expressed at high levels in spleen, thymus and leukocytes. Also expressed in lung and placenta, and at very low levels in brain, heart, skeletal muscle and kidney. Expressed in cytotoxic T-lymphocytes (CTL) and mast cells.

DISEASE:
Defects in UNC13D are the cause of hemophagocytic lymphohistiocytosis familial type 3 (FHL3) [MIM:608898]; also known as HPLH3. 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 unc-13 family.
Contains 2 C2 domains.
Contains 1 MHD1 (MUNC13 homology domain 1) domain.
Contains 1 MHD2 (MUNC13 homology domain 2) domain.

Database links:

Entrez Gene: 201294 Human

Entrez Gene: 70450 Mouse

Entrez Gene: 192177 Rat

Entrez Gene: 704431 Rhesus monkey

Omim: 608897 Human

SwissProt: Q70J99 Human

SwissProt: B2RUP2 Mouse

SwissProt: Q9R189 Rat

Unigene: 41045 Human

Unigene: 259460 Mouse

Unigene: 198919 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.ggggww.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 137大胆人体在线观看 | www.久久久久久久久久久久 | 青青青青青国产费线在线观看 | 涩涩tv| 久久这里只有精品视频99 | 国产精品久久久国产 | 猫咪在线永久网站 | 陌陌影视在线观看免费 | 大香伊人久久精品一区二区 | 一级国产精品一级国产精品片 | 日本高清免费一本视频100禁 | 忘忧草www中文在线资源 | 天天爽人人爽夜夜爽 | 中国黄色片一级 | 给我看免费播放片的视频 | 69网站在线观看 | 伊人色综合视频一区二区三区 | 日本污视频在线观看 | 欧美黑人又粗又大又爽免费 | 成人国产精品入口免费视频 | 桃色视频m3u8| 18禁无遮拦无码国产在线播放 | 亚洲永久网址在线观看 | 片多多免费观看高清 | 国产精品视频免费看 | 国产精品麻豆传媒 | 一级毛片一级黄片 | 维修工的绝遇中文字 | 2021亚洲韩国精品乱码 | 2019国产精品 | 国产高清学生妹在线观看视频一区 | 777黄色 | 国产成人XXXXX免费视频 | 国产在线一区二区三区激情欧美 | 极品少妇xxxxⅹ另类 | 3456成人看片 | 欧美性色黄大片 | 美女18禁裸乳裸体无遮挡的网站 | 色成人在线视频 | 97久久人人超碰超碰窝窝 | 久久999精品久久久 h成人在线观看 |