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
久久久久女人精品毛片,国产真人免费无码AV在线观看
Rabbit Anti-ADAMTSL2/Cy7 Conjugated antibody (bs-5862R-Cy7)
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-5862R-Cy7
英文名稱1 Rabbit Anti-ADAMTSL2/Cy7 Conjugated antibody
中文名稱 Cy7標(biāo)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  
研究領(lǐng)域 腫瘤  心血管  細(xì)胞生物  免疫學(xué)  信號轉(zhuǎn)導(dǎo)  生長因子和激素  細(xì)胞粘附分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, )
產(chǎn)品應(yīng)用
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 1mg/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 0.01M 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:
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(xì)胞外基質(zhì)蛋白
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
少妇人妻系列1~100| 欧美成人片一区二区三区| 高傲人妻女教师的沉沦长篇| 色噜噜狠狠色综合日日| 国产精品内射后入合集| 丁香色欲久久久久久综合网| av片在线观看免费| 性XXXXX大片免费视频| 国产精品色情国产三级金瓶双艳| 精品无人区无码乱码毛片国产| 国产AV国片偷人妻麻豆| 欧美交换国产一区内射| 国产乱妇无码大片在线观看| 国产成人涩涩涩视频在线观看 | 丰满的人妻hd高清日本| 无码H黄肉3D动漫在线观看| 国产H视频在线观看| 男人用嘴添女人下身免费视频| 99久久精品免费看国产| 中文字幕人成无码人妻综合社区| 99国产精品国产精品九九 | 国产乱自产黄A片在线观看| 欧美一性一乱一交一视频| 欧美最猛黑人XXXXX猛交| 狠狠色噜噜狠狠狠888米奇视频| 男女后进式猛烈XX00动态图片 | 囯产精品一品二区三区| 蜜臀AV性久久久久蜜臀AⅤ| 欧美顶级少妇做爰HD| 无码人妻AV一二区二区三区| 精品国产亚洲av麻豆| 男男又爽又黄又无遮挡网站| 色噜噜狠狠色综合久夜色撩人| 公和我在野外做好爽爱爱小说雨婷| 久久99热狠狠色AV蜜臀| 国产人妖乱国产精品人妖| jizz日本| 国产精品人妻一区夜夜爱| 杨门十二寡妇肉床艳史电影| 久久国产精品-国产精品| 日韩精品极品视频在线观看免费|