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
  
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
日韩人妻综合一区二区三区|一本加勒比HEZYO无码人妻|亚洲精品中文字幕乱码三区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-ITGA7/Cy5.5 Conjugated antibody (bs-1816R-Cy5.5)
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-1816R-Cy5.5
英文名稱1 Rabbit Anti-ITGA7/Cy5.5 Conjugated antibody
中文名稱 Cy5.5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(lǐng)域 細胞生物  免疫學  信號轉(zhuǎn)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(chǎn)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(chǎn)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(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
日韩AV无码中文字幕| 欧美XXXX黑人又粗又长精品| 最近韩国日本免费观看MV| 欧美乱大交XXXXX潮喷| 久久精品视频免费看看| 久久久久久久久久久久久久一区二区| 欧美日本免费一区二区三区| 少妇被粗大的猛烈进出免费视频| 欧美午夜精品久久久久免费视| 特级做A爰片毛片免费69| 帅小伙自慰VIDEOGAY男男| 宝宝好涨水快流出来免费视频| 蜜臀AV在线播放| 国产成人精品一区二区三区视频| 色欲AV永久无码精品无码蜜桃 | a天天插天天日| 大学生第一次破苞疼哭了| 欧美一极黄片视频一区| 日本欧美一区二区网站| 国产成人精品三级麻豆| 草草浮力影院| 久久久久夜夜夜精品国产| 性孕交大肚子孕妇| 国产黄色三级三级三级| 亚洲欧美日韩三级另类| 精品亚洲一区二区三区在线观看| 女人18片毛片60分钟| 久久综合伊人| 亚洲精品人妻在线视频| 四虎影视国产精品永久地址| 特级毛片WWW| 最近韩国日本免费高清观看| 亚洲成av人片不卡无码| 最近免费中文字幕中文高清6| 亚洲国产精久久久久久久| 艳妇系列短篇500| 久久久久亚洲精品中文字幕| 久久久久久久久久婷婷| 国产精品妇女久久久久久| 亚洲H在线播放在线观看H| 玩弄人妻少妇500系列视频|