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  人才招聘  關于我們  聯(lián)系我們
激情欧美日韩一区二区,嗯快点别停舒服好爽受不了了 ,尤物视频在线观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ADAMTSL2/Gold Conjugated antibody (bs-5862R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術支持:techsupport@xucheq.com
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-5862R-Gold
英文名稱1 Rabbit Anti-ADAMTSL2/Gold Conjugated antibody
中文名稱 膠體金標記的整合素樣金屬蛋白酶與凝血酶樣2蛋白抗體
別    名 ADAMTS like 2; ADAMTS like protein 2; ADAMTS-like protein 2; ADAMTSL 2; ADAMTSL-2; ADAMTSL2; ATL2_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  心血管  細胞生物  免疫學  信號轉導  生長因子和激素  細胞粘附分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 102kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ADAMTSL2
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
ADAMTS (A Disintegrin And Metalloproteinase Domain with Thrombospondin type 1 Modules) is a family of zinc-dependent proteases that are implicated in a variety of normal and pathological conditions, including arthritis and cancer. ADAMTS protein family members contain an amino-terminal propeptide domain, a metalloproteinase domain, a disintegrin-like domain and a carboxy-terminus that contains a varying number of Thrombospondin type 1 (TSP-1) motifs. ADAMTS-L2 (ADAMTS-like protein 2) is a 951 amino acid secreted protein that is highly expressed in lung, kidney and liver. Mutations in the gene encoding ADAMTS are the cause of geleophysic dysplasia, an autosomal recessive disorder characterized by cardiac vavular anomalies, short stature, thick skin and brachydactyly. In individuals affected with geleophysic dysplasia, there is a significant increase in total active TGF-beta 1 and nuclear locations of p-SAMD2 in fibroblasts. Interestingly, ADAMTS-L2 interacts with LTBP-1, a glycoprotein that is part of the platelet-derived TGF-beta 1 complex.

Function:
Defects in ADAMTSL2 are the cause of geleophysic dysplasia [MIM:231050]. Geleophysic dysplasia is an autosomal recessive disorder characterized by short stature, brachydactyly, thick skin and cardiac valvular anomalies often responsible for an early death.

Subcellular Location:
Secreted.

Post-translational modifications:
Glycosylated (By similarity). Can be O-fucosylated by POFUT2 on a serine or a threonine residue found within the consensus sequence C1-X(2)-(S/T)-C2-G of the TSP type-1 repeat domains where C1 and C2 are the first and second cysteine residue of the repeat, respectively. Fucosylated repeats can then be further glycosylated by the addition of a beta-1,3-glucose residue by the glucosyltransferase, B3GALTL. Fucosylation mediates the efficient secretion of ADAMTS family members. Also can be C-glycosylated with one or two mannose molecules on tryptophan residues within the consensus sequence W-X-X-W of the TPRs, and N-glycosylated. These other glycosylations can also facilitate secretion (By similarity).

DISEASE:
Defects in ADAMTSL2 are the cause of geleophysic dysplasia (GLPD) [MIM:231050]. Geleophysic dysplasia is an autosomal recessive disorder characterized by short stature, brachydactyly, thick skin and cardiac valvular anomalies often responsible for an early death.

Similarity:
Contains 1 PLAC domain.
Contains 7 TSP type-1 domains.

Database links:
UniProtKB/Swiss-Prot: Q86TH1.1

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

細胞外基質蛋白
版權所有 2004-2026 www.xucheq.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         京公網安備110107000727號
纯爱无遮挡H肉动漫在线播放| 国产欧美熟妇另类久久久| 99RE久久精品国产| 少妇无码一区二区二三区| 久久9精品区-无套内射无码| 亚洲av无码乱码在线观看性色| 午夜亚洲福利在线老司机 | 国产午夜片无码区在线播放 | 办公室丰满秘书BD正在播放| 操少妇| 国产女人被狂躁到高潮小说| 久久久亚洲精品无码| 和尚吮她的花蒂和奶水视频 | 亚洲乱码一区AV春药高潮| 天堂8在线天堂资源BT| 无码国产精品久久一区免费 | 在线观看成人网站| 高H猛烈失禁潮喷A片在线观看| 亚洲日韩精品欧美一区二区| 精品人妻人人做人人爽| 国产乱码一区二区三区| 日日噜噜噜夜夜爽爽狠狠| 兽性新人类1| 亚洲欧美激情精品一区二区| 欧美一区二区三区成人片在线| 全免费A级毛片免费看网站| 午夜精品久久久久久久久| 国产成人无码A区在线观看导航| 熟妇高潮精品一区二区三区| 啊灬啊灬啊灬免费毛片| WWXX在线观看免费| 精品久久久久久无码免费| 被夫の上司に犯中文字幕| 97人妻AV天天澡夜夜爽| 午夜一区二区国产好的精华液| 亚洲AV无码一区二区三区乱子伦 | 艳妇乳肉豪妇荡乳| 亚洲欧美日韩精品久久亚洲区| 狠狠色综合7777久夜色撩人, | 中文字幕一区二区三区乱码| 精品亚洲一区二区三区在线观看|