產(chǎn)品編號(hào) | bs-18694R-PE |
英文名稱 | Rabbit Anti-Matrilin 3/PE Conjugated antibody |
中文名稱 | PE標(biāo)記的胞外基質(zhì)蛋白3抗體 |
別 名 | AV009181; DIPOA; EDM5; HOA; MATN3; MATN3_HUMAN; Matrilin 3; Matrilin-3; OADIP; OS2. |
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 | 細(xì)胞生物 發(fā)育生物學(xué) 信號(hào)轉(zhuǎn)導(dǎo) 細(xì)胞外基質(zhì) |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Guinea Pig, Cat, ) |
產(chǎn)品應(yīng)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(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: 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 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. |
| 夜夜春亚洲嫩草直播蜜桃 | 欧美嘼交ⅹⅹⅹ╳A片 | 嫩草AV无码精品一区三区 | 亚洲高潮丝袜美女AV一区 | 外国AV无码在线观看 | 国内毛片毛片毛片毛片 | 91丝袜 国产在线观看 | 国产一区二区三区三州 | 精品三级AV在线观看入口 | 亚洲无码中文字幕国产 | 五十路近親相姦中出し親子 | 国产高潮抽搐喷白浆午夜 | 99国产精品国产免费观看 | 影音先锋男人资源av啪啪 | 泰国无码二区泰国无码三区 | 免费一级婬A片久久久爽死你网站 | 99午夜视频在线观看 | 麻豆乱码国产一区二区三区 | 国产妇女野外牲一级毛片 | 少妇特黄A一区二区三区 | 91蜜桃传媒麻豆中文字幕 | 亚洲一区二区成人精品 | 国产成人电影在线观看 | 免费在线观看黄片 | 人妻夜夜天天爽麻豆MV | 噜啊噜在线成人A片观看 | 伊人色干综合在线视频 | 喷 流水高c网站 | 国产一级a一级a爱片免费高清 | 久久久久久成人毛片免费看 | 天堂AV免费在线观看 | 特级西西4444日本少妇 | 午夜理理伦电影A片无码新新娇妻 | 国产伦精品一区二区三区视频黑人 | 白洁老师国产麻豆片 | 国产日韩一区二区三区 | 肥老熟妇伦子伦456 毛片在线免费观看视频 | 中文字幕av一区二区 | 亚洲AV无码乱码在线观看性色 | 91亚洲精品一区二区三 |