日日操日日操,亚洲一区二区三区四区视频,成人午夜福利激情,无码中文7幕

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
日韩欧洲亚洲中文,亚洲少妇中,正对逼操
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)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(chǎn)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(chǎn)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(chǎn)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 www.bklrv.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(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(wǎng)安備110107000727號
日本高清三级不卡一区| 色比合综合网| 欧美日韩中文在线观看极品| 欧美日韩人妻一区二区…| 最新偷拍女厕所久久久一区二区三区| 91guochan麻豆| 亚洲最新黄电影| 日本AⅤ123久久| 国产美腿骚逼| 啊啊啊啊在线好大| 中文字幕精品无码一 区| 国自拍区一区| 成人版91国产| 日本试看免费啊啊啊| 国产亚洲欧洲色播在线观播| 激情久久激情五月天| 美一区二区三区免费| 性色-av区| 久久久久AⅤ精品| 国产人妻精品一区二区三91| 日韩这里都是精品视频| 欧美精品综合在线| 亚洲最大成人综合网| 刺激欧美黄片在线看| 噜噜噜噜噜 久久久久| 久久妻最新资源| 男女抄B在线观看| 久久人妻在线观看| 久久日产精品一区到六区| 懂色av超碰在线| 久久久久久综合成人黄色电影| 激情午夜网站| 真实黄片视频| 草草影响中文字幕| 日韩区欧美区亚洲区| 中文字幕一区二区,日本+在线播放| 日本视频二区在线| 亚洲电影校园人妻| 大熟妇99| 人人曰麻豆精品| 久蜜av电影|