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  人才招聘  關于我們  聯(lián)系我們
午夜亚洲av影院|国产精品久久久久久无码不卡|亚洲第一无码精品一区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ITGA7/RBITC Conjugated antibody (bs-1816R-RBITC)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-1816R-RBITC
英文名稱1 Rabbit Anti-ITGA7/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的整合素α7抗體
別    名 Integrin alpha-7 heavy chain; Integrin alpha-7 70 kDa form; Integrin alpha 7; a 7; alpha7; FLJ25220; INTEGRIN ALPHA 7; ITGA7; MGC105724; ITA7_HUMAN; Integrin alpha-7; Integrin α7; Integrin-α7.  
規(guī)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  免疫學  信號轉導  干細胞  細胞粘附分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Dog, Cow, Rabbit, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 70/101/125kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Integrin alpha-7 70 kDa form
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:
The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2009]

Function:
Integrin alpha-7/beta-1 is the primary laminin receptor on skeletal myoblasts and adult myofibers. During myogenic differentiation, it may induce changes in the shape and mobility of myoblasts, and facilitate their localization at laminin-rich sites of secondary fiber formation. It is involved in the maintenance of the myofibers cytoarchitecture as well as for their anchorage, viability and functional integrity. Isoform Alpha-7X2B and isoform Alpha-7X1B promote myoblast migration on laminin 1 and laminin 2/4, but isoform Alpha-7X1B is less active on laminin 1 (In vitro). Acts as Schwann cell receptor for laminin-2. Acts as a receptor of COMP and mediates its effect on vascular smooth muscle cells (VSMCs) maturation (By similarity). Required to promote contractile phenotype acquisition in differentiated airway smooth muscle (ASM) cells.

Subunit:
Heterodimer of an alpha and a beta subunit. The alpha subunit is composed of an heavy and a light chain linked by a disulfide bond. Alpha-7 associates with beta-1. Interacts with COMP.

Subcellular Location:
Membrane; Single-pass type I membrane protein.

Tissue Specificity:
Isoforms containing segment A are predominantly expressed in skeletal muscle. Isoforms containing segment B are abundantly expressed in skeletal muscle, moderately in cardiac muscle, small intestine, colon, ovary and prostate and weakly in lung and testes. Isoforms containing segment X2D are expressed at low levels in fetal and adult skeletal muscle and in cardiac muscle, but are not detected in myoblasts and myotubes. In muscle fibers isoforms containing segment A and B are expressed at myotendinous and neuromuscular junctions; isoforms containing segment C are expressed at neuromuscular junctions and at extrasynaptic sites. Isoforms containing segments X1 or X2 or, at low levels, X1X2 are expressed in fetal and adult skeletal muscle (myoblasts and myotubes) and cardiac muscle.

Post-translational modifications:
ADP-ribosylated on at least two sites of the extracellular domain in skeletal myotubes.
A 70 kDa form is created by proteolytic cleavage. Cleavage is elevated during myogenic differentiation and the cleaved form enhances cell adhesion and spreading on laminin.

DISEASE:
Defects in ITGA7 are the cause of muscular dystrophy congenital due to integrin alpha-7 deficiency (MDCI) [MIM:613204]. A form of congenital muscular dystrophy. Patients present at birth, or within the first few months of life, with hypotonia, muscle weakness and often with joint contractures.

Similarity:
Belongs to the integrin alpha chain family. Contains 7 FG-GAP repeats.

Database links:

Entrez Gene: 3679 Human

Entrez Gene: 16404 Mouse

Entrez Gene: 81008 Rat

Omim: 600536 Human

SwissProt: Q13683 Human

SwissProt: Q61738 Mouse

SwissProt: Q63258 Rat

Unigene: 524484 Human

Unigene: 54492 Rat




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.73327.net 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(yī)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
亚洲高清自有码中文字在线观看| 精品人体无码一区二区三区| 色橹橹欧美在线观看视频高清| 少妇久久久久久久久久| 亚洲日韩欧美32p | AV大片| 日韩精品无码中文字幕一区二区 | 东北体育生巨大粗爽GAY| 中文字幕无码精品亚洲资源网久久| 日本一区二区三区夜视频| 蜜臀av国内精品久久久夜| 一本到亚洲中文无码AV| 欧美激情在线播放| 性色网站一区二区二区三| 美腿丝袜1页俺去乐| 久久精品国产亚洲av蜜臀久久| 国产成+人+亚洲+欧美+日韩| 狠狠色婷婷久久一区二区三区| 校花不着寸缕的跪趴在地下视频 | 丰满熟妇乱又伦| 亚洲熟妇少妇任你躁在线观看无码| 长长久久天天操夜夜操| 亚洲国产天堂ΑV日本国产| 高H之交换小敏系列| 日本韩国男男作爱GAYWWW| 久久综合狠狠综合久久综合88 | 人人妻人人藻人人爽欧美一区| 免费播放片Ⅴ免费人成视频| 国产日本欧美在线视频一区| 国产一产二产三精华液| 亚洲av隺v日韩精品毛片| 午夜久久久精品一区二区三区| 婷婷五月深爱五月| 下面一进一出好爽视频| 看AV免费毛片手机播放| 日韩综合一区二区视频| 成人在线免费电影| 久久99国产综合精品99| 国产精品久久人妻互换| 亚洲人精品午夜射精日韩| 欧美顶级少妇做爰HD|