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(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
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  關(guān)于我們  聯(lián)系我們
国产69精品久久久久久,狠狠色噜噜狠狠狠狠aV不卡,在线精品国产一区二区三区
Rabbit Anti-WASP/PE Conjugated antibody (bs-13681R-PE)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-13681R-PE
英文名稱 Rabbit Anti-WASP/PE Conjugated antibody
中文名稱 PE標(biāo)記的濕疹血小板減少伴免疫缺陷綜合征相關(guān)蛋白抗體
別    名 Eczema thrombocytopenia; IMD2; SCNX; THC; THC1; Thrombocytopenia 1 (X linked); U42471; Was; WASp; WASP_HUMAN; Wiskott Aldrich syndrome (eczema thrombocytopenia); Wiskott Aldrich syndrome; Wiskott Aldrich syndrome protein; Wiskott-Aldrich syndrome protein.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  細(xì)胞分化  細(xì)胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, Cow, Rabbit, )
產(chǎn)品應(yīng)用 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 53kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human WASP
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-4℃ for one year. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
The Wiskott-Aldrich syndrome (WAS) is a disorder that results from a monogenic defect that has been mapped to the short arm of the X chromosome. WAS is characterized by thrombocytopenia, eczema, defects in cell-mediated and humoral immunity and a propensity for lymphoproliferative disease. The gene that is mutated in the syndrome encodes a proline-rich protein of unknown function designated WAS protein (WASP). A clue to WASP function came from the observation that T cells from affected males had an irregular cellular morphology and a disarrayed cytoskeleton suggesting the involvement of WASP in cytoskeletal organization. Close examination of the WASP sequence revealed a putative Cdc42/Rac interacting domain, homologous with those found in PAK65 and ACK. Subsequent investigation has shown WASP to be a true downstream effector of Cdc42.

Function:
Effector protein for Rho-type GTPases, providing a link with the Arp2/3 complex that regulates the structure and dynamics of the actin cytoskeleton. Important for efficient actin polymerization. Possible regulator of lymphocyte and platelet function.

Subunit:
Interacts with NCK1 (via SH3 domains). Interacts with CDC42, RAC, NCK, HCK, FYN, SRC kinase FGR, BTK, ABL1, PSTPIP1, WIP, and to the p85 subunit of PLC-gamma. Binds the Arp2/3 complex. Interacts (via C-terminus) with ALDOA. Interacts with E.coli effector protein EspF(U).

Subcellular Location:
Cytoplasm; cytoskeleton.

Tissue Specificity:
Expressed predominantly in the thymus. Also found, to a much lesser extent, in the spleen

Post-translational modifications:
Phosphorylated at Tyr-291 by FYN and HCK, inducing WAS effector activity after TCR engagement. Phosphorylation at Tyr-291 enhances WAS activity in promoting actin polymerization and filopodia formation.

DISEASE:
Defects in WAS are the cause of Wiskott-Aldrich syndrome (WAS) [MIM:301000]; also known as eczema-thrombocytopenia-immunodeficiency syndrome.
WAS is an X-linked recessive immunodeficiency characterized by eczema, thrombocytopenia, recurrent infections, and bloody diarrhea. Death usually occurs before age 10. Defects in WAS are the cause of thrombocytopenia type 1 (THC1) [MIM:313900].
Thrombocytopenia is defined by a decrease in the number of platelets in circulating blood, resulting in the potential for increased bleeding and decreased ability for clotting.
Defects in WAS are a cause of neutropenia severe congenital X-linked (XLN) [MIM:300299]. XLN is an immunodeficiency syndrome characterized by recurrent major bacterial infections, severe congenital neutropenia, and monocytopenia.

Similarity:
Contains 1 CRIB domain.
Contains 1 WH1 domain.
Contains 1 WH2 domain.

Database links:

Entrez Gene: 7454 Human

Entrez Gene: 22376 Mouse

Omim: 300392 Human

SwissProt: P42768 Human

SwissProt: P70315 Mouse

Unigene: 2157 Human



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.ggggww.cn 北京博奧森生物技術(shù)有限公司
通過國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
主站蜘蛛池模板: 天堂av中文字幕 | av免费观看网页 | 高潮流白浆潮喷在线播放视频 | 成人无码a级毛片免费 | 日本很黄的打屁股网站 | 少妇中文字幕乱码亚洲影视 | 伊人成人在线 | 欧美成人精品网站 | 亚洲欧洲在线看 | 国产一级伦理片 | 国产资源在线观看 | 久久精品看 | 亚洲美女自拍视频 | 国产一二三四区在线 | 国产精品一级二级在线观看 | 公交车上~嗯啊被高潮视频软件 | www.俺高潮了.com | 一本伊大人香蕉久久网手机 | 日韩中文字幕在线视频观看 | 国产香蕉97碰碰久久人人九色 | 粗大的内捧猛烈进出的视频免费 | 特级黄一级播放 | 老司机狠狠干 | 国产伦精品一区二区三区综合网 | 九九九九九伊人 | japanese中年熟妇| 已婚丰满少妇21P | 精品国产人免费观看成人片 | 亚洲国产精品久久久久婷婷图片 | 网站大全免费网址 | 他掀开裙子舌头伸进去在线观看 | jk美女啪啪 | 欧美日日操| 国产人人爱 | 延禧攻略在线看 | 网友自拍露脸国语对白 | 亚洲黄色大片在线观看 | 国产亚洲一区二区视频 | 国产精品国产三级国产AV中文 | 一个色综合网 | 亚洲欧美日韩国产成人一区 |