吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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  人才招聘  關(guān)于我們  聯(lián)系我們
成人国产亚洲精品A区天堂蜜臀 ,免费无码国产欧美久久18,无码高潮又爽又黄又刺激视频
Rabbit Anti-FGF23/HRP Conjugated antibody (bs-23556R-HRP)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-23556R-HRP
英文名稱1 Rabbit Anti-FGF23/HRP Conjugated antibody
中文名稱 辣根過氧化物酶標(biāo)記的成纖維細(xì)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(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  信號轉(zhuǎn)導(dǎo)  干細(xì)胞  生長因子和激素  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse,  (predicted: Rat, )
產(chǎn)品應(yīng)用 WB=1:500-2000 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=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 mouse FGF23
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 Constituents: 0.01M PBS, pH 7.4 with 10 mg/mL BSA and 0.1% Gentamicin, 50% glycerol. Or Lyophilized. Buffer = 0.01M PBS, pH 7.4 with 10 mg/mL BSA and 0.1% Gentamicin. Reconstitute with sterile distilled water.
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 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(quán)所有 2004-2026 www.xucheq.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
中文字幕aⅴ人妻一区二区| 国产午夜片无码区在线播放| 一边摸一边做爽的视频17国产| 天天躁日日躁狠狠躁AV| 国产精品毛片久久久久久久| 夜夜嗨AV一区二区三区| AV国産精品毛片一区二区| 久久久精品一区AAA片| XXXX18一20岁HD第一次| 欧美日韩人妻精品一区二区三区| 亚洲第一成人网站| 蜜臀AV性久久久久蜜臀AⅤ| 乌克兰肥妇黑毛BBW| 苍井空AV成人片免费观看| 性欧美丰满熟妇XXXX性久久久 | 国产AV亚洲精品久久久久| 久久精品国产亚洲AV无码娇色| 小SAO货揉揉你的奶真大视频| 亚洲AV无码国产精品麻豆天美| 精品深夜AV无码一区二区| 特级毛片WWW| 亚洲av无码乱码在线观看性色| 97精品久久久久中文字幕| 99久久99久久精品国产片果冻| 日本不卡三区| 麻豆高清免费国产一区| 欧美XXXX黑人又粗又长精品| 最近高清中文在线字幕在线观看 | 欧美人与性动交CCOO| 亚洲日韩欧美一区二区三区| AV免费网站在线观看| 文中字幕一区二区三区视频播放| 99国产精品无码| 成人区色情综合小说| 国产亚洲精品无码成人| 亚洲国产精品久久久久婷婷老年| 亚洲精品午夜国产VA久久成人| 少妇被又大又粗猛烈进出视频软件 | 亚洲精品一区久久久久久| 人色偷偷色AV噜噜狠狠99| 欧美XXXX色视频在线观看|