亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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
好大好猛好深好爽视频,成年丰满熟妇午夜免费视频,亚洲国产精品久久久久婷婷软件
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-SP-C/AP Conjugated antibody (bs-10067R-AP)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-10067R-AP
英文名稱 Rabbit Anti-SP-C/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標記的肺表面活性蛋白C抗體
別    名 PSP C; PSPC; Pulmonary surfactant apoprotein 2; pulmonary surfactant apoprotein PSP C; pulmonary surfactant associated protein C; pulmonary surfactant associated proteolipid SPL pVal; Pulmonary surfactant associated proteolipid SPL(Val); SFTP 2; SFTP2; SFTPC; SFTPC surfactant pulmonary associated protein C; SP 5; SP C; SP5; SPC; surfactant associated protein pulmonary 2; Surfactant protein c; Surfactant pulmonary associated protein C; PSPC_HUMAN.  
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  細胞表面分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Cow, Rabbit, Sheep, )
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 4/21kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SP-C (24-58aa)
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 the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.

Function:
Pulmonary surfactant associated proteins promote alveolar stability by lowering the surface tension at the air-liquid interface in the peripheral air spaces.

Subcellular Location:
Secreted, extracellular space, surface film.

DISEASE:
Defects in SFTPC are the cause of pulmonary surfactant metabolism dysfunction type 2 (SMDP2) [MIM:610913]; also called pulmonary alveolar proteinosis due to surfactant protein C deficiency. A rare disease associated with progressive respiratory insufficiency and lung disease with a variable clinical course, due to impaired surfactant homeostasis. It is characterized by alveolar filling with floccular material that stains positive using the periodic acid-Schiff method and is derived from surfactant phospholipids and protein components. Excessive lipoproteins accumulation in the alveoli results in severe respiratory distress.
Genetic variations in SFTPC are a cause of susceptibility to respiratory distress syndrome in premature infants (RDS) [MIM:267450]; also known as RDS in prematurity. RDS is a lung disease affecting usually premature newborn infants. It is characterized by deficient gas exchange, diffuse atelectasis, high-permeability lung edema and fibrin-rich alveolar deposits called 'hyaline membranes'.

Similarity:
Contains 1 BRICHOS domain.

Database links:

Entrez Gene: 6440 Human

Entrez Gene: 20389 Mouse

Omim: 178620 Human

SwissProt: P11686 Human

SwissProt: P21841 Mouse

Unigene: 1074 Human

Unigene: 24040 Mouse



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.www.chomd.com.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: 色综合视频一区二区三区57| 久久久精品人妻一区二区三区四区金瓶梅| 国产成人精品午夜福利电影|波多久久亚| 成人精品一区二区三区中文字幕_| 中文字幕乱码久久午夜乱码 | 人妻无码中文字幕按摩番号| 精品久久久久久成人热,91| 成年美女黄网站色大片不卡下载| 亚洲一区二区三区香蕉一本道| 人妻大战黑人白浆狂泄视频| 国产AⅤ无码旗袍丝袜美腿在线看| 一本色道久久综合亚洲精品主演 | 日韩精品专区在线影院重磅_日韩精品一区二区亚洲AV | 亚洲高清毛片一区二区柏| 精品久久久久久久久久久院品网| 18禁美女裸体免费网站扒内衣久久 | 无码av大香线蕉久久竹菊| 国产在线观看高清精品8X| 亚洲一本之道高清,亚洲| 久久国乱精品| 一级做a爰片性色毛片免费网站少 一级做a爰全过程免费视频,日韩一区二区三区四区区区 | 久一久无码毛片永久网站| 99久久亚洲精品无码毛片,无码国产999精品久久久 | 久久不见久久见免费视频粉色视频| 自拍亚洲一区二区三区在线| 一本在线无码com| 久久99精品久久久久久久不卡99精品久久久久中文 | 国产91在线九色视频露脸| 亚洲风间由美无码一区| 国产探花在线视频乳春色红桃视频| 亚洲精品无码一区二区三区污 | 免费精品一区二区三区第35二区抖阴 | 亚洲乱码少妇99P-=三四区| 精品无码久久久久国产影视大全| 一区二区三区久久精品网| 精品国产亚洲一区二区三区,中文字字幕 | 99精品国产99久久久久久久久久 | 中文字幕久久综合久久优播 | 特级做a爰片毛片免费96视频| XXXX日本永久免费视频入口| 人妻japanesefree人妻|