91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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(lián)系我們
国产免费一区二区一羞羞视频,精品国产91乱码一区二区三区 ,国产成人精品无码
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-HCP1/Cy5.5 Conjugated antibody (bs-15428R-Cy5.5)
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-15428R-Cy5.5
英文名稱 Rabbit Anti-HCP1/Cy5.5 Conjugated antibody
中文名稱 Cy5.5標記的血紅素轉運蛋白1抗體
別    名 G21; HCP 1; Heme Carrier Protein 1; MGC9564; PCFT; PCFT/HCP1; PCFT_HUMAN; PDE7A; Proton coupled folate transporter; Proton-coupled folate transporter; SLC46A1; Solute carrier family 46 member 1;   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  細胞生物  免疫學  信號轉導  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Cow, )
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 50kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HCP1
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 transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]

Function:
Has been shown to act both as an intestinal proton-coupled high-affinity folate transporter and as an intestinal heme transporter which mediates heme uptake from the gut lumen into duodenal epithelial cells. The iron is then released from heme and may be transported into the bloodstream. Dietary heme iron is an important nutritional source of iron. Shows a higher affinity for folate than heme.

Subcellular Location:
Apical cell membrane; Multi-pass membrane protein. Cytoplasm. Note=Localizes to the apical membrane of intestinal cells in iron-deficient cells, while it resides in the cytoplasm in iron-replete cells.

Tissue Specificity:
Expressed in kidney, liver, placenta, small intestine, spleen, retina and retinal pigment epithelium. Lower levels found in colon and testis. Very low levels in brain, lung, stomach, heart and muscle. In intestine, expressed in duodenum with lower levels in jejunum, ileum, cecum, rectum and segments of the colon.

DISEASE:
Hereditary folate malabsorption (HFM) [MIM:229050]: Rare autosomal recessive disorder characterized by impaired intestinal folate absorption with folate deficiency resulting in anemia, hypoimmunoglobulinemia with recurrent infections, and recurrent or chronic diarrhea. In many patients, neurological abnormalities such as seizures or mental retardation become apparent during early childhood, attributed to impaired transport of folates into the central nervous system. When diagnosed early, the disorder can be treated by administration of folate. If untreated, it can be fatal and, if treatment is delayed, the neurological defects can become permanent. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the major facilitator superfamily. SLC46A family.

Database links:

Entrez Gene: 5781 Human

Entrez Gene: 19247 Mouse

Entrez Gene: 25622 Rat

Omim: 176876 Human

SwissProt: Q06124 Human

SwissProt: P35235 Mouse

SwissProt: P41499 Rat

Unigene: 506852 Human

Unigene: 474046 Mouse

Unigene: 8681 Mouse

Unigene: 98209 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 rvdoil.com 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(yī)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
男人的天堂久久2024 | 蜜桃亚洲AV无码一区二区三区 | 红桃视频成人免费无码 | 在线中文字幕观看 | 中文无码人妻AV素人 | 中文字幕无码人妻在线视频 | 欧美一级特黄A片免费观看密森 | 久久成年人视频免费 | 永久免费在线看黄网站 | 91超碰在线播放 | ,国产乱人伦无无码视频 | 亚洲无遮挡国产视频 | 日本成熟人妻理伦无码新片 | 国产一级a毛一级a毛观看视频网站 | 91亚洲精品久久久久蜜桃 | 成人性爱在线观看 | 欧美性爱一区二区三区 | a片视频免费在线观看 | 午夜影院在线免费观看 | 人人婷婷人人澡人人妻 | 国产精品海角社区在线观看 | 国产精品久久久久AV | 少妇又紧又色又爽又刺激视频 | 精品女同A片中文字幕 | 娇喘91丨丨白浆秘 | 自慰在线观看第一页 | 麻豆传媒在线观看国产 | 少妇激情偷人爽爽91嫩草 | 永久免费的网站在线观看黄 | 欧美一区二区三区高潮菊竹 | 欧美A片全裸在线视频 | 免费在线观看一区二区 | 一级婬片试看15分钟水多 | 日本黑人乱偷人妻中文 | 成人在线一区二区三区 | 四川BBB搡BBB搡多人孕妇 | 免费中文字幕在线观看 | 久久国产精品波多野结衣AV孕妇 | 亚洲欧美动漫偷拍 | 少妇又紧又湿又深又爽麻豆 | 午夜日韩射精福利在线观看 |