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(hào)           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
成人免费无码成人影院日韩,亚洲成AV人片在线观看无
Rabbit Anti-MMP13/Cy5 Conjugated antibody (bs-0575R-Cy5)
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(jià)
產(chǎn)品編號(hào) bs-0575R-Cy5
英文名稱1 Rabbit Anti-MMP13/Cy5 Conjugated antibody
中文名稱 Cy5標(biāo)記的基質(zhì)金屬蛋白酶13抗體
別    名 CLG 3; CLG3; Collagenase 3; Collagenase3; MMP13; MMP 13; MMP-13; Matrix Metalloproteinase 13; MMP 13; MMP13_HUMAN.   
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 腫瘤  心血管  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞骨架  細(xì)胞外基質(zhì)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse, Rat,  (predicted: Rabbit, )
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 52kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MMP13
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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:
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The protein encoded by this gene cleaves type II collagen more efficiently than types I and III. It may be involved in articular cartilage turnover and cartilage pathophysiology associated with osteoarthritis. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3. [provided by RefSeq, Jul 2008].

Function:
Degrades collagen type I. Does not act on gelatin or casein. Could have a role in tumoral process.

Subcellular Location:
Secreted, extracellular space, extracellular matrix (Probable).

Tissue Specificity:
Seems to be specific to breast carcinomas.

DISEASE:
Defects in MMP13 are the cause of spondyloepimetaphyseal dysplasia Missouri type (SEMD-MO) [MIM:602111]. A bone disease characterized by moderate to severe metaphyseal changes, mild epiphyseal involvement, rhizomelic shortening of the lower limbs with bowing of the femora and/or tibiae, coxa vara, genu varum and pear-shaped vertebrae in childhood. Epimetaphyseal changes improve with age.
Defects in MMP13 are the cause of metaphyseal anadysplasia type 1 (MANDP1) [MIM:602111]. Metaphyseal anadysplasia consists of an abnormal bone development characterized by severe skeletal changes that, in contrast with the progressive course of most other skeletal dysplasias, resolve spontaneously with age. Clinical characteristics are evident from the first months of life and include slight shortness of stature and a mild varus deformity of the legs. Patients attain a normal stature in adolescence and show improvement or complete resolution of varus deformity of the legs and rhizomelic micromelia.

Similarity:
Belongs to the peptidase M10A family.
Contains 4 hemopexin-like domains.

Database links:

Entrez Gene: 4322 Human

Entrez Gene: 17386 Mouse

Entrez Gene: 171052 Rat

Entrez Gene: 403763 Dog

Omim: 600108 Human

SwissProt: P45452 Human

SwissProt: P33435 Mouse

SwissProt: P23097 Rat



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

MMP13基質(zhì)金屬蛋白酶-13可降解Ⅰ、Ⅱ、Ⅲ型膠原,并對(duì)Ⅱ型膠原更有效果,主要用于骨與關(guān)節(jié)病變的研究。
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(hào): 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(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
一区二区三区| 玩弄人妻少妇500系列视频| 欧美日韩免费做爰大片人| 亚洲国产精品久久人人爱| 伊人WWW22综合色| 99久久国产露脸精品竹菊传媒| 国产精品一区二区AV| 国产成人精品无码一区二区 | 蜜臀AV性久久久久蜜臀AⅤ| 久久久久人妻精品一区三寸| 女人18毛片A级毛片| 欧美黑人添添高潮A片WWW| 厨房掀起少妇裙子挺进去| 老旺的大肉蟒进进出出| 久久人妻少妇嫩草AV蜜桃| 无码日本精品XXXXXXXXX| 扒开腿狂躁女人爽出白浆| 无码人妻丰满熟妇区BBBBXXXX | 少妇无码一区二区二三区| 亚洲国产精品无码中文在线| 免费无码毛片一区二区APP| 斗罗大陆在线全集免费看| 秘书喂奶好爽一边吃奶一| 久久久久亚洲精品无码蜜桃| jizz日本| 国产无套内射又大又猛又粗又爽 | 熟妇人妻av无码一区二区三区| H高潮娇喘抽搐A片国产麻豆 | 国产特黄A片AAAA毛片| 亚洲乱码一区AV春药高潮| 亚洲AV无码国产精品久久不卡| 欧美军警GAY巨大粗长| 人妻 丝袜美腿 中文字幕| 麻豆AV天堂一二三区视频| 男人J桶进女人P无遮挡全过程| 国产精品v欧美精品v日韩精品| av无码久久久久久不卡网站| 无码粉嫩虎白一线天在线观看| 妺妺窝人体色WWW看人体| 疯狂做受XXXX高潮欧美日本| 国产精品免费无遮挡无码永久视频 |