强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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(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
国产一区二区三区三区在线观看,国产suv精品一区二区6
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
human CD45 (bsm-30095M-PerCP-Cy5.5)  
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
25T/2200.00元
50T/3680.00元
100T/4900.00元
大包裝/詢價
產(chǎn)品編號 bsm-30095M-PerCP-Cy5.5
英文名稱 human CD45
中文名稱 PerCP-Cy5.5標記的小鼠抗人CD45單克隆抗體
別    名 B220; CD 45; CD-45; cd45 antigen; ec3.1.3.48; CD45R; GP180; GP180; GP 180; L CA; LCA; L-CA; Leukocyte common antigen; LY5; Ly-5 glycoprotein; Protein tyrosine phosphatase receptor type C; Protein tyrosine phosphatase receptor type c polypeptide; protein tyrosine phosphatase, receptor type, C; Receptor-type tyrosine-protein phosphatase C; PTPRC; PTPRC_HUMAN; SCID due to PTPRC deficiency; T200; T200 glycoprotein; T200 leukocyte common antigen; Human homolog of severe combined immunodeficiency due to PTPRC deficiency.  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 HI30
交叉反應(yīng) Human
產(chǎn)品應(yīng)用 Flow-Cyt=10ul/Test
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
細胞定位 細胞膜 
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 Recombinant human CD45 
亞    型 Mouse IgG1, k
純化方法 affinity purified by Protein G
緩 沖 液 0.01M PBS (pH7.4), 0.5% BSA, 0.02% Proclin300.
保存條件 Store at 2-8℃. Protect from light. Avoid freezing.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus belongs to receptor type PTP. This gene is specifically expressed in hematopoietic cells. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes, or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and thus functions as a regulator of cytokine receptor signaling

Function:
Protein tyrosine-protein phosphatase required for T-cell activation through the antigen receptor. Acts as a positive regulator of T-cell coactivation upon binding to DPP4. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits and dephosphorylates SKAP1 and FYN. Dephosphorylates LYN, and thereby modulates LYN activity.

Subunit:
Binds GANAB and PRKCSH. Interacts with SKAP1. Interacts with DPP4; the interaction is enhanced in a interleukin-12-dependent manner in activated lymphocytes. Contains 2 tyrosine-protein phosphatase domains.

Subcellular Location:
Membrane; Single-pass type I membrane protein. Membrane raft. Note=Colocalized with DPP4 in membrane rafts.

Post-translational modifications:
Heavily N- and O-glycosylated.

DISEASE:
Defects in PTPRC are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (T(-)B(+)NK(+) SCID) [MIM:608971]. A form of severe combined immunodeficiency (SCID), a genetically and clinically heterogeneous group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. Patients present in infancy recurrent, persistent infections by opportunistic organisms. The common characteristic of all types of SCID is absence of T-cell-mediated cellular immunity due to a defect in T-cell development. Genetic variations in PTPRC are involved in multiple sclerosis susceptibility (MS) [MIM:126200]. MS is a neurodegenerative disorder characterized by the gradual accumulation of focal plaques of demyelination particularly in the periventricular areas of the brain. Peripheral nerves are not affected. Onset usually in third or fourth decade with intermittent progression over an extended period. The cause is still uncertain.

Similarity:
Belongs to the protein-tyrosine phosphatase family. Receptor class 1/6 subfamily. Contains 2 fibronectin type-III domains. Contains 2 tyrosine-protein phosphatase domains.

Database links:

Entrez Gene : 5788 Human

Entrez Gene : 19264 Mouse

Entrez Gene : 24699 Rat

Omim : 151460 Human

SwissProt : P08575 Human

SwissProt : P06800 Mouse

SwissProt : P04157 Rat

Unigene : 654514 Human

Unigene : 391573 Mouse

Unigene : 90166 Rat



CD45在活化信號轉(zhuǎn)導中起到調(diào)節(jié)作用,在確定CD45為一種PTPase之前就已證實了CD45參于細胞的活化和生長調(diào)節(jié)。
抗CD45抗體可以抑制PHA或CD3交聯(lián)所介導的T細胞增殖,還可抑制NK或細胞毒性T細胞對靶細胞的殺傷,抑制經(jīng)CD2、CD3以及CD8膜分子介導的信號轉(zhuǎn)導作用。
版權(quán)所有 2004-2026 www.nmgps.com 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
精品无码免费人侵犯AV | 91麻豆产精品久久久久久 | 再深点灬舒服灬免费A片 | 欧美乱战大交XXXXX | 黄网视频在线欢看 | 水户香奈中文字幕无码 | 欧一美一交一配一交一交一视一频 | 99re国产精品 | 亚洲AV无码乱码精品 | 免费 无码 无套内谢软件 | 婬乱的妇女HD中文字幕 | 有码无码国产在线播放 | 看国产熟妇乱子伦 | 国产乱码日产乱码精品精 | 亚洲AV无码蜜桃希岛爱理 | 少妇w搡BBB搡BBB出血 | bbb午夜专区在线观看 | 精品久久久久久久久久久久 | 四季AV一区二区三区免费观看 | 与子亂倫刺激對白 | 3D区无码区动漫区一区二区三区 | 富婆一级婬片A片AAA毛片91 | 国产熟妇婬乱一区二区 | 无码人妻AⅤ一区二区三区鲁大师 | 成人视频免费在线观看 | 久久99久久99精品 | 特级老太婆婬片A片 | www.久久久久久久 | 欧美午夜在线观看视频 | 精品国产美女裸身无遮挡AV上网站 | 国产伦精品一区二区免费 | 久久久精品一区二区三区 | 国产一级AA无码大片 | 国产高清在线观看 | 少妇无码免费精品不卡AV专区 | 天天躁日日躁AAAAXXXX | 无码免费人妻A片AAA毛片西瓜 | 成人网站在线观看一区高清 | 国产成人无码久久久久毛片朴信惠 | 国产剧情亚洲无码视频 | 91久久夜色精品国产九色杨思敏 |