来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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
亚洲欧美日韩在线不卡|国产在线国偷精品免费看|男女裸体做爰爽爽全过程
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Rabbit Anti-SPP24  antibody (bs-8518R)  
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產(chǎn)品編號 bs-8518R
英文名稱 Rabbit Anti-SPP24  antibody
中文名稱 分泌性磷蛋白24抗體
別    名 Secreted phosphoprotein 24; Spp-24; Secreted phosphoprotein 2; SPP2; SPP-2; SPP 2; SPP24_HUMAN.  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  激酶和磷酸酶  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human)
產(chǎn)品應(yīng)用 ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
細(xì)胞定位 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPP24/SPP2: 55-160/211 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 SPP24, also known as secreted phosphoprotein 2, is a 211 amino acid secreted protein that belongs to the cystatin superfamily. Expressed in liver and plasma, SPP24 may play a role in coordinating an aspect of bone turnover. The gene that encodes SPP24 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

Subcellular Location:
Secreted.

Tissue Specificity:
Detected in liver and plasma.

Similarity:
Belongs to the SPP2 family.

SWISS:
Q13103

Gene ID:
6694

Database links:




版權(quán)所有 2004-2026 www.73327.net 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
99精品日韩欧美在线观看| 不许人间见白头| 在线无码视频观看草草视频| 日本高清一区2区三区| 搡BBBB搡BBB搡| 六月婷婷国产精品综合| 国产成人精品无码专区| 亚洲AV第一成肉网| 久久人人爽天天玩人人妻精品| 日进去了啊内射视频| 扒开老师大腿猛进AAA片| 艳妇乳肉豪妇荡乳AV| 双胞胎(H)互攻| 免费乱肥胖伦老女人| 亚洲性无码一区二区三区| 欧美三级A做爰在线观看 | 2018高清日本一道国产-在| 天天做天天爱夜夜爽毛片毛片,| 无人视频在线观看完整版高清| 无码人妻少妇色欲AV一区二区| 一区二区三区久久久久久久久久| 久久久久亚洲精品无码蜜桃| 国产精品永久久久久久久久久| 免费大黄网站在线观| 草草成年视频在线播放| 中文字幕久区久久中文字幕 | 99国产精品国产精品九九| 亚洲人成亚洲人成在线观看| 欧美大片一区二区三区| 久久久精品一区AAA片| 艳妇系列短篇500| 中文字幕2017| 国产欧美一区二区三区久久久| 人妻精品久久久久中文字幕| 韩国免费A级作爱片免费观看中国 色噜噜AV亚洲色一区二区 | 亚洲超碰无码色中文字幕97| 久久精品A亚洲国产V高清不卡| 熟女中文字幕一区二区| 国产成人精品免费青青草原| 一夲道无码人妻精品一区二区| 国产亚洲色婷婷久久99精品|