超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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
欧美视频在线第一页,婷婷色香合缴缴情av第三区,国产农村妇女高潮大叫
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Laminin Beta 2/PE-Cy3 Conjugated antibody (bs-7504R-PE-Cy3)
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-PE-Cy3
英文名稱 Rabbit Anti-Laminin Beta 2/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3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.ggggww.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: 中文字幕天天躁日日躁狠狠躁 | 亚洲av片不卡无码影视 | 亚洲成年女人av毛片性性教育 | 久久久久久色 | 韩国三级黄色毛片 | 免费一级A级高清毛片 | 在线综合亚洲 | 国色天香综合网 | 欧美精品 | 成人美女免费网站视频 | 欧美久久一级片 | 在线国产福利精品 | 国产熟熟 | oae裸神系列88av | 天天干天天射天天操天天摸 | 国产精品自产拍在线免费看 | 爆乳女仆高潮在线观看 | 欧美精品久久久久久久影视 | 国产日本一区 | 日本aaaa片毛片免费观看视频 | oae裸神系列88av | ww久久| 无码一卡二卡三卡四卡 | 中国一级特黄真人毛片免费观看 | 亚洲精品美女久久777777 | 欧美日韩黄视频 | 日本边添边摸边做边爱边 | 久久99国产精品 | 蘑菇视频黄色 | 囯产无码大放纵视频 | 国产精品美女久久久久久久久久久 | 日本三级欧美三级人妇视频黑白配 | 538国产精品一区二区免费视频 | 我要看免费的毛片 | 性xxxxfreexxxxx | 亚洲一二三区在线观看 | 成人aa片免费观看视频 | 亚洲天堂久久新 | 在线观看人成 | 亚洲精品久久久久久久久久吃药 | 人人综合亚洲无线码另类 |