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(guān)注公眾號           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
艳妇肉交dvideos,少妇激情偷人爽爽91嫩草,国产熟睡乱子伦午夜视频在线
Rabbit Anti-HCP1/BF350 Conjugated antibody (bs-15428R-BF350)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號 bs-15428R-BF350
英文名稱 Rabbit Anti-HCP1/BF350 Conjugated antibody
中文名稱 BF350標(biāo)記的血紅素轉(zhuǎn)運(yùn)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(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 心血管  細(xì)胞生物  免疫學(xué)  信號轉(zhuǎn)導(dǎo)  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Cow, )
產(chǎn)品應(yīng)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(quán)所有 2004-2026 rvdoil.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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
精品国产乱码久久久久久1区2区-亚洲 | 91丨国产丨精品入口男男 | 媚黑无码视频一区二区 | 国产乱国产乱老熟300视频 | 欧美丰满少妇猛烈进入A片蜜桃 | 四川少妇BBBBBB爽爽爽欧美 | 国产精品操操黑料影院 | 国产三级午夜理伦三级 | 特黄a又粗又大又黄又爽A片麻豆 | 熟妇女人妻呻吟久久AV | 麻豆91精品91久久久 | 久久久国产精品免费A片蜜 欧美性猛交 XX 乱下载 | 色哟哟 国产精品色哟哟 | 欧美成人午夜无码A片秀色直播 | 国产又粗又硬又长又爽 | 国产粉嫩极品美女 | 国产一级a毛一级a看免费视频乱 | 午夜17c网暴精品人妻 | 亚洲精品在线观看视频 | 国产肥白大熟妇BBBB | 欧–美–性–交–黄–片 | 日本理论片午伦夜理片更新时间 | 亚洲精品无码久久久 | 免费看国产女人动态图片 | 国产精品乱码一区二区免费视频 | 国产高清免费在线观看 | 日韩精品少妇无码一区二区三区 | 2018精品爱爱视频 | 中文人妻熟妇精品乱又伧老牛在线 | 国产一级一级毛片 | 国产成人无码免费视频 | 无码人妻一区二区三区在线 | 色欲狠狠躁天天躁无码中文字幕 | 久久成人网一区二区青椒直播 | 成人午夜做爰高潮片免费吸气 | 国产黄A片免费网站免费 | 九九成人网免费视频 | 一级婬片120分钟试看 | 91在线无码精品秘 传媒 | 国产伦精品一区二区三毛 | 国产成人中文网站 |