来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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
亚洲女性午夜福利视频|国产真实迷奷在线观看|蜜臀AV在线
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Matrilin 3/Cy7 Conjugated antibody (bs-18694R-Cy7)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-18694R-Cy7
英文名稱1 Rabbit Anti-Matrilin 3/Cy7 Conjugated antibody
中文名稱 Cy7標記的胞外基質(zhì)蛋白3抗體
別    名 AV009181; DIPOA; EDM5; HOA; MATN3; MATN3_HUMAN; Matrilin 3; Matrilin-3; OADIP; OS2.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  發(fā)育生物學(xué)  信號轉(zhuǎn)導(dǎo)  細胞外基質(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
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(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

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(quán)所有 2004-2026 www.73327.net 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
熟女俱乐部五十路六十路AV| 九九在线免费视频精品| 妺妺窝人体色WWW看美女| 国产精品久久久久久96| 亚洲一区欧美一区中文精品| 成人毛片18女人毛片免费看| 小视频在线观看| AV中文无码在线| GOGOGO日本免费观看视频| 亚洲国产成人精品无码区在线观看| 一区二区三区亚洲av电影| 国产在线观看a视频| 亚洲熟妇欲望一二三区av| 性色AV无码不卡中文字幕| 天天干夜夜操狠狠插用力撞| CHINESE老女人老熟妇HD| 孩交精品XXXX视频视频| 国产精品揄拍100视频| 亚洲AV综合色区无码一区爱AV| 欧美黑人添添高潮A片WWW| 欧美a一级片日日爱| 色综合99久久久无码国产精品| 熟妇与小伙子MATUR老熟妇E| 91精品国产亚一区二区三区 | 亚洲日韩免费成人AV| 在办公室伦流澡到高潮H| 高清在线播放| 国产乱理伦片在线观看夜| 日本精品无码久久久久三级国产 | 女朋友水太多进去就软了| 久久久中日AB精品综合| 亚洲日韩AV无码| 欧美老妇交乱视频| 天天躁日日躁狠狠躁AV麻豆 | 无码专区中文字幕无码野外| 国产传媒果冻天美传媒怎么入职| 久久EE热这里只有精品| 色噜噜狠狠色综合久夜色撩人| 国产精品成人一区二区不卡| 中文字幕aⅴ人妻一区二区| 成人精品天堂一区二区三区|