强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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
亚洲国产精品久久久,国产丨熟女丨国产熟女视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-FGF23/PE-Cy3 Conjugated antibody (bs-5768R-PE-Cy3)
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-5768R-PE-Cy3
英文名稱 Rabbit Anti-FGF23/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3標記的成纖維細胞生長因子23抗體
別    名 ADHR; FGF-23; Fgf23; FGF 23; FGF23_HUMAN; Fibroblast growth factor 23; Fibroblast growth factor 23 N-terminal peptide; Fibroblast growth factor 23 precursor; HPDR2; HYPF; Phosphatonin; PHPTC; Tumor derived hypophosphatemia inducing factor; Tumor-derived hypophosphatemia-inducing factor.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  信號轉導  干細胞  生長因子和激素  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Rat,  (predicted: Human, Mouse, Dog, Pig, Cow, Horse, Rabbit, Sheep, Guinea Pig, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 27kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Fibroblast growth factor 23 N-terminal peptide
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 member of the fibroblast growth factor family of proteins, which possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. The product of this gene regulates phosphate homeostasis and transport in the kidney. The full-length, functional protein may be deactivated via cleavage into N-terminal and C-terminal chains. Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR). Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC). [provided by RefSeq, Feb 2013]

Function:
Regulator of phosphate homeostasis. Inhibits renal tubular phosphate transport by reducing SLC34A1 levels. Upregulates EGR1 expression in the presence of KL. Acts directly on the parathyroid to decrease PTH secretion. Regulator of vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization.

Subunit:
Interacts with FGFR1, FGFR2, FGFR3 and FGFR4. Affinity between fibroblast growth factors (FGFs) and their receptors is increased by KL and heparan sulfate glycosaminoglycans that function as coreceptors.

Subcellular Location:
Secreted. Note=Secretion is dependent on O-glycosylation.

Tissue Specificity:
Expressed in osteogenic cells particularly during phases of active bone remodeling. In adult trabecular bone, expressed in osteocytes and flattened bone-lining cells (inactive osteoblasts).

Post-translational modifications:
Following secretion this protein is inactivated by cleavage into a N-terminal fragment and a C-terminal fragment. The processing is effected by proprotein convertases.
O-glycosylated by GALT3. Glycosylation is necessary for secretion; it blocks processing by proprotein convertases when the O-glycan is alpha 2,6-sialylated. Competition between proprotein convertase cleavage and block of cleavage by O-glycosylation determines the level of secreted active FGF23.

DISEASE:
Defects in FGF23 are the cause of autosomal dominant hypophosphataemic rickets (ADHR) [MIM:193100]. ADHR is characterized by low serum phosphorus concentrations, rickets, osteomalacia, leg deformities, short stature, bone pain and dental abscesses.
Defects in FGF23 are a cause of hyperphosphatemic familial tumoral calcinosis (HFTC) [MIM:211900]. HFTC is a severe autosomal recessive metabolic disorder that manifests with hyperphosphatemia and massive calcium deposits in the skin and subcutaneous tissues.

Similarity:
Belongs to the heparin-binding growth factors family.

Database links:

Entrez Gene: 8074 Human

Omim: 605380 Human

SwissProt: Q9GZV9 Human

Unigene: 287370 Human



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 m.nmgps.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(wǎng)安備110107000727號
久久久精品一区二区三区 | 老汉好大灬好硬灬好爽灬无码 | 亚洲中文字幕4444 | 被老师摁着强国产最新黄色无码视频 | 亚洲无码一区二区三区 | 国产精品成人在线 | 无遮挡XX00动态图120秒 | 色情肉欲奶头无码A片 | 国产精品翘臀性爱视频 | 欧美性猛交XXX乱大交3蜜桃 | 99国产精品在线观看 | 麻豆国产91 在线播放 | 国产91九色足控脚交在线播放 | 国产在线观看国产精品产拍 | 少妇也疯狂毛毛毛毛A片 | 亚洲精品免费在线 | 国模吧一区二区三区 | 粉嫩小泬BBBB免费看 | 亚洲欧美一二三区91蜜桃臀久久一区 | 亚洲婷婷一本高清 | 国产成人无码精品色欲天香 | 日韩欧美在线视频观看 | 久久久久中精品中文字幕 | 欧美一区二区三区爱爱 | 中文字幕无码一区二区黑人巨大 | 又紧又大又粗又硬又长视频 | 女生自慰白丝在线观看 | 国产一区二区在线看 | 四川少妇搡BBw搡BBBB搡 | 99久久精品国产波多野结衣图片 | 91精品人妻无码系列九色 | 国产精品久久久一级毛片 | 天天影视色欲综合插插插 | 波多野结衣20次连续高潮 | 91色成人少妇无码精品 | 要灬要灬再深点受不了混乱 | 蜜桃mv在线mv免费mv香蕉 | 四川少妇搡bbbb搡bbbb | 国产主播在线观看一区二区不卡av | 欧美一级婬片A片免费手机版 | 岳伦一区二区三区在线播放 |