97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

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  關于我們  聯系我們
艹逼软件免费,亚洲一区免费在线,日本激情网址
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Laminin Beta 2/BF647 Conjugated antibody (bs-7504R-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-7504R-BF647
英文名稱 Rabbit Anti-Laminin Beta 2/BF647 Conjugated antibody
中文名稱 BF647標記的層粘連蛋白β2抗體
別    名 LAMB2; Laminin beta 2; Laminin subunit beta 2; LAMS; S laminin; LAMB2_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  神經生物學  細胞粘附分子  細胞骨架  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Cow, Horse, Rabbit, Sheep, .)
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 192kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Laminin Beta 2/Laminin S
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:
Laminin S binds to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. Laminin S is a complex glycoprotein, consisting of three different polypeptide chains (alpha, beta, gamma), which are bound to each other by disulfide bonds into a cross-shaped molecule comprising one long and three short arms with globules at each end. Beta 2 is a subunit of laminin 3 (Laminin S), laminin 4 (S merosin), and laminin 7 (KS laminin).

Function:
Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.

Subunit:
Laminin is a complex glycoprotein, consisting of three different polypeptide chains (alpha, beta, gamma), which are bound to each other by disulfide bonds into a cross-shaped molecule comprising one long and three short arms with globules at each end. Beta-2 is a subunit of laminin-3 (laminin-121 or S-laminin), laminin-4 (laminin-221 or S-merosin), laminin-7 (laminin-321 or KS-laminin), laminin-9 (laminin-421), laminin-11 (laminin-521), laminin-14 (laminin-423) and laminin-15 (laminin-523).

Subcellular Location:
Secreted, extracellular space, extracellular matrix, basement membrane. Note=S-laminin is concentrated in the synaptic cleft of the neuromuscular junction.

DISEASE:
Defects in LAMB2 are the cause of Pierson syndrome (PIERSS) [MIM:609049]; also known as microcoria-congenital nephrotic syndrome. Pierson syndrome is characterized by nephrotic syndrome with neonatal onset, diffuse mesangial sclerosis and eye abnormalities with microcoria as the leading clinical feature. Death usually occurs within the first weeks of life. Disease severity depends on the mutation type: nontruncating LAMB2 mutations may display variable phenotypes ranging from a milder variant of Pierson syndrome to isolated congenital nephrotic syndrome.
Defects in LAMB2 are the cause of nephrotic syndrome type 5 with or without ocular abnormalities (NPHS5) [MIM:614199]. NPHS5 is a renal disease characterized clinically by proteinuria, hypoalbuminemia, hyperlipidemia and edema. Kidney biopsies show non-specific histologic changes such as focal segmental glomerulosclerosis and diffuse mesangial proliferation. Some affected individuals have an inherited steroid-resistant form and progress to end-stage renal failure. NPHS5 is characterized by very early onset of progressive renal failure. A subset of patients may develop mild ocular anomalies, such as myopia, nystagmus, and strabismus.

Similarity:
Contains 13 laminin EGF-like domains.
Contains 1 laminin IV type B domain.
Contains 1 laminin N-terminal domain.

Database links:

Entrez Gene: 3913 Human

Entrez Gene: 3909 Human

Entrez Gene: 3914 Human

Entrez Gene: 3918 Human

SwissProt: P55268 Human

SwissProt: Q13751 Human

SwissProt: Q13753 Human

SwissProt: Q16787 Human

SwissProt: Q61087 Mouse

SwissProt: Q61092 Mouse

SwissProt: Q61789 Mouse



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.kastlife.cn 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
主站蜘蛛池模板: 大地资源在线观看免费高清动漫 | 国产一区三 | 国产日本在线视频 | 国产一区国产二区在线观看 | 日韩欧美大片在线观看 | 色婷婷成人综合激情免费视频 | 成全动漫在线观看免费高清 | 精品乱子伦一区日本午夜 | 欧美日韩亚洲天堂 | 国产亚洲日韩A欧美在线人成 | 欧美综合视频在线 | 国产精品免费视频二三区 | 午夜一级黄色大片 | 国内不卡的一区二区三区中文字幕 | 禁断一区二区三区在线 | 亚洲欧美精品一中文字幕 | 无码精品人妻一区二区三区老牛 | 精品无码国产污污污免费网站 | 日本韩国三级aⅴ在线观看 日本视频免费 | 日韩欧美大片在线观看 | 亚洲黄色网页 | 九色新网址 | 亚洲V国产V天堂A无码二区 | 四虎亚洲精品私库AV在线 | 天堂在线www资源在线 | 国产一级淫片a按摩推澡按摩 | 小小拗女一区二区三区 | 欧洲成人一区 | 一级毛片免费播放 | 毛片a片免费看 | 在线观看欧美日韩国产 | 久久精品天堂 | 日日夜夜精品网站 | 亚洲国产成人精品无码区在线网站 | 欧美视频1区 | 日本永久免费a∨在线视频 91精品国产综合久久小仙女图片 | 久久不见久久见中文字幕免费 | 亚人在线播放国产中文字幕 | 成熟人妻换╳╳╳╳ | 一区二区三区四区日韩 | 成人日韩精品 |