99精品欧美一区二区三区综合在线,国产精品一区二区的,欧美亚洲国产日韩综合,99精品视频在线观看2

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  關(guān)于我們  聯(lián)系我們
国产精品国产三级国产剧情,成人黄色小视频下载网站
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
TGFBI Recombinant Rabbit mAb (bsm-54085R)  
~~~促銷,代碼KT202504~~~
訂購熱線:400-901-9800
訂購郵箱:sales@www.eweiwc.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.eweiwc.cn
25ul/800.00元
50ul/1400.00元
100ul/2500.00元
大包裝/詢價

產(chǎn)品編號 bsm-54085R
英文名稱 TGFBI Recombinant Rabbit mAb
中文名稱 角膜上皮蛋白TGFBI重組兔單抗
別    名 AI181842; AI747162; beta ig; beta ig h3; beta ig-h3; BGH3_HUMAN; Big h3; BIGH3; CDB1; CDG2; CDGG1; CSD; CSD1; CSD2; CSD3; EBMD; Kerato epithelin; Kerato-epithelin; LCD1.  
研究領(lǐng)域 細胞生物  發(fā)育生物學  神經(jīng)生物學  信號轉(zhuǎn)導  干細胞  生長因子和激素  
抗體來源 Rabbit
克隆類型 Recombinant
交叉反應(yīng) Human,Mouse (predicted: Rat)
產(chǎn)品應(yīng)用 WB=1:500-1000,IHC-P=1:100-500,IHC-F=1:400-800,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 72 kDa
檢測分子量
細胞定位 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TGFBI 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 This gene encodes an RGD-containing protein that binds to type I, II and IV collagens. The RGD motif is found in many extracellular matrix proteins modulating cell adhesion and serves as a ligand recognition sequence for several integrins. This protein plays a role in cell-collagen interactions and may be involved in endochondrial bone formation in cartilage. The protein is induced by transforming growth factor-beta and acts to inhibit cell adhesion. Mutations in this gene are associated with multiple types of corneal dystrophy. [provided by RefSeq, Jul 2008]

Function:
Binds to type I, II, and IV collagens. This adhesion protein may play an important role in cell-collagen interactions. In cartilage, may be involved in endochondral bone formation.

Subcellular Location:
Secreted > extracellular space > extracellular matrix. May be associated both with microfibrils and with the cell surface. Tissue Specificity : Highly expressed in the corneal epithelium.

Post-translational modifications:
Gamma-carboxyglutamate residues are formed by vitamin K dependent carboxylation. These residues are essential for the binding of calcium.

DISEASE:
Defects in TGFBI are the cause of epithelial basement membrane corneal dystrophy (EBMD) [MIM:121820]; also known as Cogan corneal dystrophy or map-dot-fingerprint type corneal dystrophy. EBMD is a bilateral anterior corneal dystrophy characterized by grayish epithelial fingerprint lines, geographic map-like lines, and dots (or microcysts) on slit-lamp examination. Pathologic studies show abnormal, redundant basement membrane and intraepithelial lacunae filled with cellular debris. Although this disorder usually is not considered to be inherited, families with autosomal dominant inheritance have been identified.
Defects in TGFBI are the cause of corneal dystrophy Groenouw type 1 (CDGG1) [MIM:121900]; also known as corneal dystrophy granular type. Inheritance is autosomal dominant. Corneal dystrophies show progressive opacification of the cornea leading to severe visual handicap.
Defects in TGFBI are the cause of corneal dystrophy lattice type 1 (CDL1) [MIM:122200]. Inheritance is autosomal dominant.
Defects in TGFBI are a cause of corneal dystrophy Thiel-Behnke type (CDTB) [MIM:602082]; also known as corneal dystrophy of Bowman layer type 2 (CDB2). Defects in TGFBI are the cause of Reis-Buecklers corneal dystrophy (CDRB) [MIM:608470]; also known as corneal dystrophy of Bowman layer type 1 (CDB1). Defects in TGFBI are the cause of lattice corneal dystrophy type 3A (CDL3A) [MIM:608471]. CDL3A clinically resembles to lattice corneal dystrophy type 3, but differs in that its age of onset is 70 to 90 years. It has an autosomal dominant inheritance pattern.
Defects in TGFBI are the cause of Avellino corneal dystrophy (ACD) [MIM:607541]. ACD could be considered a variant of granular dystrophy with a significant amyloidogenic tendency. Inheritance is autosomal dominant.

Similarity:
Contains 1 EMI domain.
Contains 4 FAS1 domains.

SWISS:
Q15582

Gene ID:
7045

產(chǎn)品圖片
Western blot analysis of TGFBI on different lysates with Rabbit anti-TGFBI antibody (bsm-54085R) at 1/500 dilution. Lane 1: Mouse eyeball tissue lysate Lane 2: Mouse colon tissue lysate Lysates/proteins at 20 μg/Lane. Predicted band size: 75 kDa Observ
Immunohistochemical analysis of paraffin-embedded human uterus tissue using anti-TGFBI antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30
Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue using anti-TGFBI antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BS
Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue using anti-TGFBI antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA
Immunohistochemical analysis of paraffin-embedded human liver carcinoma tissue using anti-TGFBI antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BS
版權(quán)所有 2004-2026 www.www.eweiwc.cn 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
国产在线中文字幕一区二区三区| 怎么样操女人的逼亚洲Av黄片段| 精品福利一区二区三区在线观看| 操女人逼逼骚逼逼| 日韩亚洲AV无码一区二区不卡| 大鸡吧天天草黑逼| 这里只有久久精品| 九九在线视频热线视频精选| 成人男女做爰免费视频网| 非洲大鸡巴操逼黄色录像| 中日美女毛5片一区二区三区| 成人黄色精品久久app| 日韩人妻无码中字一区二区| 日韩成人伦理片在线观看| 女人被躁到高潮嗷嗷叫小| 日本一区二区三区四区五| 在线无码一区二区三区不卡| 最新的精品亚洲一区二区| 国产精品无码一二区免费| 在线观看国产日韩欧美一区二区| 一区二区国产精品免费视频| 日韩中文字幕一区二区高清| 国产精品三二一免费| 亚洲av伦理一区二区三区久久| 男生舔女生下面黄色视频| 大胸美女被c的嗷嗷叫视频| 国产精品亚洲一区二区三区极品| 在线视频观看一区| 被下药强奷到舒服的视频| 男生和女人靠逼视频| 国产精品熟女一区二区三区久久夜| 黑人巨茎和中国美女视频| 天天干天天操天天插| 国产熟女视频一区二区三区| 女人日比比视频免费| 插女人下面高潮视频| 高清无码精品一区二区三区| 野外日逼视频免费看| 国产午夜精品美女视频露脸| 九九视频这里只有精品| 啊好爽好多水深插射视频|