超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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  關于我們  聯系我們
亚洲精品自在在线观看,好男人在线影院官网WWW,美女狠狠操
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Matrilin 3/RBITC Conjugated antibody (bs-18694R-RBITC)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-18694R-RBITC
英文名稱 Rabbit Anti-Matrilin 3/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的胞外基質蛋白3抗體
別    名 AV009181; DIPOA; EDM5; HOA; MATN3; MATN3_HUMAN; Matrilin 3; Matrilin-3; OADIP; OS2.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  發育生物學  信號轉導  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Guinea Pig, Cat, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 53kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Matrilin 3
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.
產品介紹 background:
This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins is thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This protein contains two von Willebrand factor A domains; it is present in the cartilage extracellular matrix and has a role in the development and homeostasis of cartilage and bone. Mutations in this gene result in multiple epiphyseal dysplasia. [provided by RefSeq, Jul 2008]

Function:
Major component of the extracellular matrix of cartilage and may play a role in the formation of extracellular filamentous networks.

Subcellular Location:
Secreted.

Tissue Specificity:
Expressed only in cartilaginous tissues, such as vertebrae, ribs and shoulders.

DISEASE:
Defects in MATN3 are the cause of multiple epiphyseal dysplasia type 5 (EDM5) [MIM:607078]. EDM is a generalized skeletal dysplasia associated with significant morbidity. Joint pain, joint deformity, waddling gait, and short stature are the main clinical signs and symptoms. EDM is broadly categorized into the more severe Fairbank and the milder Ribbing types. EDM5 is relatively mild and clinically variable. It is primarily characterized by delayed and irregular ossification of the epiphyses and early-onset osteoarthritis.
Defects in MATN3 are the cause of spondyloepimetaphyseal dysplasia MATN3-related (SEMD-MATN3) [MIM:608728]. A bone disease characterized by disproportionate early-onset dwarfism, bowing of the lower limbs, lumbar lordosis and normal hands. Skeletal abnormalities include short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, hypoplastic iliac bones and flat, ovoid vertebral bodies.
Genetic variations in MATN3 are associated with susceptibility to osteoarthritis type 2 (OS2) [MIM:140600]; also called osteoarthritis of distal interphalangeal joints (OADIP) or hand osteoarthritis (HOA). Osteoarthritis is a degenerative disease of the joints characterized by degradation of the hyaline articular cartilage and remodeling of the subchondral bone with sclerosis. Clinical symptoms include pain and joint stiffness often leading to significant disability and joint replacement. In the hand, osteoarthritis can develop in the distal interphalangeal and the first carpometacarpal (base of thumb) and proximal interphalangeal joints. Patients with osteoarthritis may have one, a few, or all of these sites affected.

Similarity:
Contains 4 EGF-like domains.
Contains 1 VWFA domain.

Database links:

Entrez Gene: 4148 Human

Entrez Gene: 17182 Mouse

Entrez Gene: 313954 Rat

Omim: 602109 Human

SwissProt: O15232 Human

SwissProt: O35701 Mouse

Unigene: 656199 Human

Unigene: 42226 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.ggggww.cn 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
主站蜘蛛池模板: 亚洲一二三中文字幕 | 天堂一区二区三区 | 色欲AV午夜一区二区三区 | 国产三级精品三级在线专区 | 久草在线青青草 | 黄色片视频免费在线观看 | 麻豆国产在线播放 | 亚洲国产精品区 | 在线免费观看黄网 | 国产91精品高清一区二区三区 | 免费久草| 中国老太老妇xx对白 | 国产成a人片在线观看视频99 | 91精品久久久久久久久不卡 | 午夜观看视频 | 欧美婷婷六月丁香综合色 | 香蕉久久人人爽人人爽人人片av | 精品午夜一区二区 | 日本线在线 | 韩国一级片| 不卡一二三 | 天堂中文视频在线 | 日本精品久久 | com.黄 | 好吊日好吊操在线 | 老头玩小嫩奶陈晴晴老刘 | 午夜裸体女人视频网站在线观看 | 天堂网成人在线 | 相泽南av日韩在线 | 天天操天天干天天曰 | 一级毛片大片 | 一级片国产片 | 国产午夜福利片1000无码 | 无码中文字幕AV带剧情 | 成人在线免费观看视频网站 | 欧亚精品卡一卡二卡三 | 亚洲欧美日韩国产高清在线观看 | 国产91高清在线 | 在线观看免费视频91 | 2019亚洲天堂 | 中国少妇xx|