日日操日日操,亚洲一区二区三区四区视频,成人午夜福利激情,无码中文7幕

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
歐美精品久久久婷婷中文在线,88国产精品免费一区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Kindlin/Biotin Conjugated antibody (bs-17063R-Bio)
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-17063R-Bio
英文名稱 Rabbit Anti-Kindlin/Biotin Conjugated antibody
中文名稱 生物素標記的整合素相互作用蛋白Kindlin抗體
別    名 C20orf42; Chromosome 20 open reading frame 42; DTGCU 2; DTGCU2; FERM1_HUMAN; Fermitin family homolog 1; Fermt1; FLJ20116; FLJ23423; KIND 1; KIND1; Kinderlin; Kindlerin; Kindlin 1; Kindlin syndrome protein; Kindlin-1; Kindlin1; Unc 112 related protein 1; Unc-112-related protein 1; Unc112 related protein; UNC112A; URP 1; URP1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  腫瘤細胞生物標志物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Horse, Rabbit, Sheep, )
產品應用 WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 77kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Kindlin
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:
This gene encodes a member of the fermitin family, and contains a FERM domain and a pleckstrin homology domain. The encoded protein is involved in integrin signaling and linkage of the actin cytoskeleton to the extracellular matrix. Mutations in this gene have been linked to Kindler syndrome. [provided by RefSeq, Dec 2009]

Function:
Involved in cell adhesion. Contributes to integrin activation. When coexpressed with talin, potentiates activation of ITGA2B. Required for normal keratinocyte proliferation. Required for normal polarization of basal keratinocytes in skin, and for normal cell shape. Required for normal adhesion of keratinocytes to fibronectin and laminin, and for normal keratinocyte migration to wound sites. May mediate TGF-beta 1 signaling in tumor progression.

Subcellular Location:
Cytoplasm > cytoskeleton. Cell junction > focal adhesion. Cell projection > ruffle membrane. Constituent of focal adhesions. Localized at the basal aspect of skin keratinocytes, close to the cell membrane. Colocalizes with filamentous actin. Upon TGFB1 treatment, it localizes to membrane ruffles.

Tissue Specificity:
Expressed in brain, skeletal muscle, kidney, colon, adrenal gland, prostate, and placenta. Weakly or not expressed in heart, thymus, spleen, liver, small intestine, bone marrow, lung and peripheral blood leukocytes. Overexpressed in some colon and lung tumors. In skin, it is localized within the epidermis and particularly in basal keratocytes. Not detected in epidermal melanocytes and dermal fibroblasts.

DISEASE:
Defects in FERMT1 are the cause of Kindler syndrome (KINDS) [MIM:173650]. An autosomal recessive skin disorder characterized by skin blistering, photosensitivity, progressive poikiloderma, and extensive skin atrophy. Additional clinical features include gingival erosions, ocular, esophageal, gastrointestinal and urogenital involvement, and an increased risk of mucocutaneous malignancy. Note=Although most FERMT1 mutations are predicted to lead to premature termination of translation, and to loss of FERMT1 function, significant clinical variability is observed among patients. There is an association of FERMT1 missense and in-frame deletion mutations with milder disease phenotypes, and later onset of complications (PubMed:21936020).

Similarity:
Belongs to the kindlin family.
Contains 1 FERM domain.
Contains 1 PH domain.

Database links:

Entrez Gene: 55612 Human

Entrez Gene: 524427 Cow

Entrez Gene: 241639 Mouse

Omim: 607900 Human

SwissProt: Q9BQL6 Human

SwissProt: P59113 Mouse

Unigene: 472054 Human

Unigene: 209784 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Kindlin家族是新近發(fā)現的粘著斑蛋白(focal adhesion protein),有3個成員(Kindlin-1、Kindlin-2、Kindlin-3)。Kindlin家族參與整合素活化、細胞遷移、增殖和分化的調控,在臨床上與皮膚疾病發(fā)生、腫瘤的侵襲、心血管生成、免疫系統功能有密切關系。Kindlins異??梢詫е露喾N遺傳性疾病,如Kindlin-1功能異常導致Kindler綜合征(Kindler syndrome,KS)和Kindlin-3功能異常導致白細胞黏附缺陷(1eukocyte adhesion deficiency,LAD—HI)。目前已在人類實體腫瘤(乳腺癌、前列腺癌、平滑肌肉瘤)中發(fā)現Kindlin-2與腫瘤的侵襲性及耐藥性有關。
版權所有 2004-2026 www.bklrv.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(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
欧美喷水XXX| 欧美色成人综合天天综合| 玖玖99永远| 91内射白| 97超碰99热| 一区精品 - 百度| 日韩欧美不良网站在线观看视频| 一级欧美欧美日韩视频| 久久国产伦理电影| www免费午夜福利| 午夜婷婷五月天在线| 免费av一区在线观看| 久久a热| 小黄书成人精品91| 九一av电影| 中国无码在线观看91中文字幕| 日韩视频图一图二视频| 欧美爽爽精品| a√不卡无码高清片| 亚洲 欧美 国产 图片| 又大又粗又爽国产| 免费h自拍| 天堂黄片免费| 欧美日韩国产 123| 中文无码网导航| 国产3p激情自拍| 欧美亚洲日韩一本| 亚洲图片欧美狂野| 久久麻豆伦理久久久久| 欧美色影院| 日本黄色伦理网站| 成人亚洲一区成人欧美| 欧美亚洲女成人| 久久电影婷婷| 日本视频在线一区二区三区| 日韩成人区| 日韩精品电影网站| 久久久少妇42P| 一区二区三区黄片在线视频观看 | 国产一区无码中出| 亚洲人妻五月婷婷|