mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關(guān)注公眾號(hào)           掃碼咨詢(xún)技術(shù)支持           掃碼咨詢(xún)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  人才招聘  關(guān)于我們  聯(lián)系我們
亚洲午夜精品一区二区蜜桃,欧美日韩一区久久久久久,国产亚洲精品久久飘花
首頁(yè) > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Rabbit Anti-HRAS  antibody (bs-1071R)  
~~~促銷(xiāo)代碼KT202411~~~
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@m.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說(shuō)明書(shū): 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢(xún)價(jià)

產(chǎn)品編號(hào) bs-1071R
英文名稱(chēng) Rabbit Anti-HRAS  antibody
中文名稱(chēng) 原癌基因H-ras抗體
別    名 c bas/has; c H ras; c has/bas p21 protein; C K RAS; c K ras2 protein; c Ki ras; c Kirsten ras protein; c ras Ki 2 protein; Cellular c Ki ras2 proto oncogene antibody G1III6 N ras; GTPase HRas; GTPase KRas; GTPase NRas; H Ras 1; H RasIDX; Ha Ras; HRAS 1; HRAS; HRAS1; K Ras 2; K ras; K ras p21 protein; K RAS2A; K RAS2B; K RAS4A; K RAS4B; KI RAS; Kirsten rat sarcoma 2 viral (v Ki ras2) oncogene homolog; KRAS 1; KRAS 2; KRAS; KRAS1; KRAS2; N ras; N ras oncogene; Neuroblastoma RAS viral (v ras) oncogene homolog; NRAS 1; NRAS; NRAS1; NS3; Oncogene KRAS2; p21ras; PR310 c K ras oncogene antibody RASH 1; RASH1; RASK 2; RASK2; Transforming protein N Ras; Transforming protein p21; v Ha ras Harvey rat sarcoma viral oncogene homolog; v Ki ras2 Kirsten rat sarcoma 2 viral oncogene homolog; v Ki ras2 Kirsten rat sarcoma viral oncogene homolog; v ras neuroblastoma RAS viral oncogene homolog; RASH_HUMAN.  
Specific References  (3)     |     bs-1071R has been referenced in 3 publications.
[IF=1.994] DAN-PING XIEet al. Anti-tumor Properties of Picrasma quassioides Extracts in H-RasG12V Liver Cancer Are Mediated Through ROS-dependent Mitochondrial Dysfunction. ANTICANCER RESEARCH 40: 3819-3830 (2020)  WB ;  Human.  
[IF=1.994]   WB ;  human.  
[IF=1.785] Gui-Nan Shen. et al. The compound 2?benzylthio?5,8?dimethoxynaphthalene?1,4?dione leads to apoptotic cell death by increasing the cellular reactive oxygen species levels in Ras?mutated liver cancer cells. Exp Ther Med. 2020 Nov;20(5):1-1  WB ;  Mouse.  
研究領(lǐng)域 腫瘤  免疫學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  結(jié)合蛋白  
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng) Human,Mouse,Rat (predicted: Rabbit,Chicken)
產(chǎn)品應(yīng)用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 21kDa
細(xì)胞定位 細(xì)胞核 細(xì)胞漿 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human H-ras: 101-152/189 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) 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 This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, mental retardation, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants, which encode different isoforms, have been identified for this gene. [provided by RefSeq].

Function:
Ras proteins bind GDP/GTP and possess intrinsic GTPase activity.

Subunit:
In its GTP-bound form interacts with PLCE1. Interacts with TBC1D10C. Interacts with RGL3. Interacts with HSPD1. Found in a complex with at least BRAF, HRAS1, MAP2K1, MAPK3 and RGS14. Interacts (active GTP-bound form) with RGS14 (via RBD 1 domain) (By similarity). Forms a signaling complex with RASGRP1 and DGKZ. Interacts with RASSF5. Interacts with PDE6D. Interacts with IKZF3. Interacts with GNB2L1.

Subcellular Location:
Cell membrane. Cell membrane; Lipid-anchor; Cytoplasmic side. Golgi apparatus. Golgi apparatus membrane; Lipid-anchor. Note=The active GTP-bound form is localized most strongly to membranes than the inactive GDP-bound form (By similarity). Shuttles between the plasma membrane and the Golgi apparatus.
Isoform 2: Nucleus. Cytoplasm. Cytoplasm, perinuclear region. Note=Colocalizes with GNB2L1 to the perinuclear region.

Tissue Specificity:
Widely expressed.

Post-translational modifications:
Palmitoylated by the ZDHHC9-GOLGA7 complex. A continuouscycle of de- and re-palmitoylation regulates rapid exchange betweenplasma membrane and Golgi.
S-nitrosylated; critical for redox regulation. Important forstimulating guanine nucleotide exchange. No structural perturbationon nitrosylation.
The covalent modification of cysteine by15-deoxy-Delta12,14-prostaglandin-J2 is autocatalytic andreversible. It may occur as an alternative to other cysteinemodifications, such as S-nitrosylation and S-palmitoylation.
Acetylation at Lys-104 prevents interaction with guaninenucleotide exchange factors (GEFs) (By similarity).

DISEASE:
Faciocutaneoskeletal syndrome (FCSS) [MIM:218040]: A rarecondition characterized by prenatally increased growth, postnatalgrowth deficiency, mental retardation, distinctive facialappearance, cardiovascular abnormalities (typically pulmonicstenosis, hypertrophic cardiomyopathy and/or atrial tachycardia),tumor predisposition, skin and musculoskeletal abnormalities.Note=The disease is caused by mutations affecting the generepresented in this entry.
Congenital myopathy with excess of muscle spindles(CMEMS) [MIM:218040]: Variant of Costello syndrome. Note=Thedisease is caused by mutations affecting the gene represented inthis entry.
Hurthle cell thyroid carcinoma (HCTC) [MIM:607464]: Arare type of thyroid cancer accounting for only about 3-10% of alldifferentiated thyroid cancers. These neoplasms are considered avariant of follicular carcinoma of the thyroid and are referred toas follicular carcinoma, oxyphilic type. Note=Diseasesusceptibility is associated with variations affecting the generepresented in this entry.
Note=Mutations which change positions 12, 13 or 61activate the potential of HRAS to transform cultured cells and areimplicated in a variety of human tumors.
Bladder cancer (BLC) [MIM:109800]: A malignancyoriginating in tissues of the urinary bladder. It often presentswith multiple tumors appearing at different times and at differentsites in the bladder. Most bladder cancers are transitional cellcarcinomas that begin in cells that normally make up the innerlining of the bladder. Other types of bladder cancer includesquamous cell carcinoma (cancer that begins in thin, flat cells)and adenocarcinoma (cancer that begins in cells that make andrelease mucus and other fluids). Bladder cancer is a complexdisorder with both genetic and environmental influences.Note=Disease susceptibility is associated with variations affectingthe gene represented in this entry.
Note=Defects in HRAS are the cause of oral squamous cellcarcinoma (OSCC).
Schimmelpenning-Feuerstein-Mims syndrome (SFM)[MIM:163200]: A disease characterized by sebaceous nevi, often onthe face, associated with variable ipsilateral abnormalities of thecentral nervous system, ocular anomalies, and skeletal defects.Many oral manifestations have been reported, not only includinghypoplastic and malformed teeth, and mucosal papillomatosis, butalso ankyloglossia, hemihyperplastic tongue, intraoral nevus, giantcell granuloma, ameloblastoma, bone cysts, follicular cysts,oligodontia, and odontodysplasia. Sebaceous nevi follow the linesof Blaschko and these can continue as linear intraoral lesions, asin mucosal papillomatosis. Note=The disease is caused by mutationsaffecting the gene represented in this entry.

Similarity:
Belongs to the small GTPase superfamily. Ras family.

SWISS:
P01112

Gene ID:
3265

Database links:

Entrez Gene: 3265 Human

Entrez Gene: 15461 Mouse

Entrez Gene: 293621 Rat

Omim: 190020 Human

SwissProt: P01112 Human

SwissProt: Q61411 Mouse

SwissProt: P20171 Rat

Unigene: 37003 Human

Unigene: 334313 Mouse

Unigene: 102180 Rat



GDP/GTP結(jié)合蛋白(GDP/GTP Bijding Protein)
細(xì)胞信號(hào)轉(zhuǎn)導(dǎo)系統(tǒng)紊亂是腫瘤細(xì)胞生長(zhǎng)的重要特征之一,Ras蛋白參與體內(nèi)多種細(xì)胞信號(hào)轉(zhuǎn)導(dǎo)途徑而發(fā)揮作用,而原癌基因H-ras是一種多功能的細(xì)胞因子,廣泛存在于自然界,H-ras在多種細(xì)胞生命活動(dòng)中起極為重要的作用,包括細(xì)胞的增殖、分化和細(xì)胞骨架的構(gòu)建等等,該抗體主要用于腫瘤方面的研究。
產(chǎn)品圖片
Tissue/cell: rat brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; Incubation: Anti-HRAS/Ras/Ras p21 Polyclonal Antibody, Unconjugated(bs-1071R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
Tissue/cell: rat lung tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; Incubation: Anti-HRAS/Ras/Ras p21 Polyclonal Antibody, Unconjugated(bs-1071R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
版權(quán)所有 2004-2026 www.m.p2b3.cn 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产日欧一片内射午夜| 人妻互换免费中文字幕| 中文字幕最新在线资源| 国产精品日本欧美一区二区三区| 日本午夜羞羞在线观看| 亚洲国产精品一区二区三区久久| 人妻夜夜爽天天爽精品三区| 久久久精品熟女亚洲av麻豆| 中文字幕亚洲一区巨区| 一区二区日韩av激情| 亚洲国产电影一区二区三区| 日本一区二区三区影院| 国产69精品久久久久久老妇| 亚洲伦理精品国产成人一区| 亚洲国产精品午夜福利久久| 接下来开始上伦理课免费观看| 91国产精品免费观看| 97人人妻人人澡人人爽| 亚洲综合网无码中文字幕| 日日摸夜夜摸狠狠摸婷婷| 国产日韩欧美精品小视频| 国产精品视频二区不卡| 国产精品久久久久久久久三级| 日本电影三级一区二区三区| 色婷婷狠狠久久综合五月| 亚洲精品国产第一区三区| 亚洲精品成人18久久| 无码人妻视频一区二区三区| 久久久久国产精品老熟女| 国产又粗又长又硬又黄网站| 久久国产无码模特视频| 欧美一区二区三区啪啪| 亚洲国产精品一区二区三区久久| 欧洲日韩在线观看一区二区三区视频| 久久久久蜜桃成人精品一区| 午夜亚洲在在线观看| 日本精品va在线观看| 国产又长有粗的视频| 日本一区二区三区四区.| 五月婷婷六月丁香综合小说| 日韩欧美精品在线中文字幕|