欧美精品日韩在线视频-久久视频精彩在线观看-精品少妇人妻一区二区黑-欧美日韩中文字幕人妻-丁香九月婷婷综合在线-久久久亚洲熟妇熟女一区-久久久久免费看片-日本中文字幕人妻少妇在线-女同久久另类99精品国产,欧美 另类 自拍偷拍,中文字幕人妻系列懂色av,久久久亚洲精品男人的天堂

首頁(yè) > 抗體 > 一抗 > 其它 > RAG-2 Monoclonal Antibody
RAG-2 Monoclonal Antibody
商品貨號(hào)： PLA005010
適 應(yīng) 性： 人
WB ELISA
￥600元
規(guī)格：
在線咨詢
MSDS
說(shuō)明書(shū)
商品描述
  • 發(fā)貨日期： 7
  • 基因名稱： RAG2
  • 蛋白名稱： V(D)J recombination-activating protein 2
  • Human_gene_id： 5897
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5897
  • Human_swiss_prot_no： P55895
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/P55895/entry
  • Mouse_swiss_prot_no： P21784
  • Mouse_swiss_link： http://www.uniprot.org/uniprot/P21784
  • 特異性： RAG-2 Monoclonal Antibody detects endogenous levels of RAG-2 protein.
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來(lái)源： Monoclonal, Mouse
  • 稀釋： WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
  • 純化工藝： Affinity purification
  • 儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說(shuō)明書(shū)： 1
  • Msds： MSDS_Antibody.pdf
  • 其他名稱： RAG2; V(D)J recombination-activating protein 2; RAG-2
  • 信號(hào)通路： Primary immunodeficiency;
  • 功能： disease:Defects in RAG2 are a cause of combined cellular and humoral immune defects with granulomas (CHIDG) [MIM:233650]. CHIDG is an immunodeficiency disease with granulomas in the skin, mucous membranes, and internal organs. Other characteristics include hypogammaglobulinemia, a diminished number of T and B cells, and sparse thymic tissue on ultrasonography.,disease:Defects in RAG2 are a cause of Omenn syndrome (OS) [MIM:603554]; a severe immunodeficiency characterized by the presence of activated, anergic, oligoclonal T-cells, hypereosinophilia, and high IgE levels.,disease:Defects in RAG2 are a cause of severe combined immunodeficiency, autosomal recessive T cell-negative, B-cell-negative, NK cell-positive (T(-)B(-)NK(+)SCID) [MIM:601457]. SCID refers to 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 with SCID present in infancy with 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.,function:During lymphocyte development, the genes encoding immunoglobulins and T-cell receptors are assembled from variable (V), diversity (D), and joining (J) gene segments. This combinatorial process, known as V(D)J recombination, allows the generation of an enormous range of binding specificities from a limited amount of genetic information. The RAG1/RAG2 complex initiates this process by binding to the conserved recombination signal sequences (RSS) and introducing a double-strand break between the RSS and the adjacent coding segment. These breaks are generated in two steps, nicking of one strand (hydrolysis), followed by hairpin formation (transesterification). RAG1/2 has also been shown to function as a transposase in vitro, and to possess RSS-independent endonuclease activity (end processing) and hairpin opening. RAG1 alone can bind to RSS but stable, efficient binding requires RAG2. All known catalytic activities require the presence of both proteins.,online information:RAG2 deficiency database,similarity:Belongs to the RAG2 family.,subunit:The RAG complexes appear to contain three to five molecules of RAG2 for each molecule of RAG1.,tissue specificity:Cells of the B- and T-lymphocyte lineages.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Nucleus .
  • 組織表達(dá)： Cells of the B- and T-lymphocyte lineages.
  • 科研貨號(hào)： PLA005010
RAG-2 Monoclonal Antibody
Catalog No PLA005010
Product information
  • 發(fā)貨日期： 7
  • 基因名稱： RAG2
  • 蛋白名稱： V(D)J recombination-activating protein 2
  • Human_gene_id： 5897
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5897
  • Human_swiss_prot_no： P55895
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/P55895/entry
  • Mouse_swiss_prot_no： P21784
  • Mouse_swiss_link： http://www.uniprot.org/uniprot/P21784
  • 特異性： RAG-2 Monoclonal Antibody detects endogenous levels of RAG-2 protein.
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來(lái)源： Monoclonal, Mouse
  • 稀釋： WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
  • 純化工藝： Affinity purification
  • 儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說(shuō)明書(shū)： 1
  • Msds： MSDS_Antibody.pdf
  • 其他名稱： RAG2; V(D)J recombination-activating protein 2; RAG-2
  • 信號(hào)通路： Primary immunodeficiency;
  • 功能： disease:Defects in RAG2 are a cause of combined cellular and humoral immune defects with granulomas (CHIDG) [MIM:233650]. CHIDG is an immunodeficiency disease with granulomas in the skin, mucous membranes, and internal organs. Other characteristics include hypogammaglobulinemia, a diminished number of T and B cells, and sparse thymic tissue on ultrasonography.,disease:Defects in RAG2 are a cause of Omenn syndrome (OS) [MIM:603554]; a severe immunodeficiency characterized by the presence of activated, anergic, oligoclonal T-cells, hypereosinophilia, and high IgE levels.,disease:Defects in RAG2 are a cause of severe combined immunodeficiency, autosomal recessive T cell-negative, B-cell-negative, NK cell-positive (T(-)B(-)NK(+)SCID) [MIM:601457]. SCID refers to 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 with SCID present in infancy with 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.,function:During lymphocyte development, the genes encoding immunoglobulins and T-cell receptors are assembled from variable (V), diversity (D), and joining (J) gene segments. This combinatorial process, known as V(D)J recombination, allows the generation of an enormous range of binding specificities from a limited amount of genetic information. The RAG1/RAG2 complex initiates this process by binding to the conserved recombination signal sequences (RSS) and introducing a double-strand break between the RSS and the adjacent coding segment. These breaks are generated in two steps, nicking of one strand (hydrolysis), followed by hairpin formation (transesterification). RAG1/2 has also been shown to function as a transposase in vitro, and to possess RSS-independent endonuclease activity (end processing) and hairpin opening. RAG1 alone can bind to RSS but stable, efficient binding requires RAG2. All known catalytic activities require the presence of both proteins.,online information:RAG2 deficiency database,similarity:Belongs to the RAG2 family.,subunit:The RAG complexes appear to contain three to five molecules of RAG2 for each molecule of RAG1.,tissue specificity:Cells of the B- and T-lymphocyte lineages.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Nucleus .
  • 組織表達(dá)： Cells of the B- and T-lymphocyte lineages.
  • 科研貨號(hào)： PLA005010
    • Hunan UPT Biotechnology Co.,Ltd
    Website：www.hyjdss.com Servive hotline :4006916686
    E-mail：service@uptbio.com
    Address：
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
普拉特澤實(shí)驗(yàn)室電話助手

4006916686

掃碼咨詢

岛国av在线播放视频-在线免费观看中文字幕2021-欧美巨大性爽欧美精品一-丁香色婷婷综合激情 | 91看成免人成电影-大香蕉久久综合一区-中文字幕制服丝袜人妻熟女-久久95热在精品国产 | 天天日天天操天天干天天摸-麻豆高清在线视频免费观看-日韩免费a视频-91人人妻人人澡人 | 国产精品久久久久久色婷婷-精品人妻少妇av一区二区-国产精品中文字幕视频-青青久久美女视频 | 99国产区二区视频在线观看-精品久久久999久久久-日韩欧美一区二区三区四区五区-久久久久国产精品一级黄片 | 日韩最新在线观看视频-91人妻中文在线一区二区三区-国模福利视频在线观看-国产精品va尤物在线观看 | 亚洲天堂中文字幕悠悠-久久夜久久久久-久久久久亚洲av毛片大全有-日韩欧美国产免费大片 | 91成人自拍视频在线-日本人妻丰满熟妇久久久久-亚洲av大岛优香作品在线观看-日韩精品在线视频观看 | 久久6精品视频-人人干人人插人人艹-日韩高清砖码一二三区-成人国产精品一入口免费视频 | 中文字幕人妻中出在线一区-久久精品亚洲午夜-久久久久久久一区二-丝袜亚洲精品中文字幕 | 丁香六月婷婷视频在线-最新中文字幕版av-精品一区二区久久久久久久的-97人人妻精品 | 国产精品久久久久69粉嫩-熟女人妻精品一区二区三区四区-日本偷拍精品久久久-婷婷久久在线观看视频 | 超碰caoporn免费-精品人妻一区二区三区蜜桃乌龙-国产一区二区三区御姐-精品久久久久久久久中文字幕 | 精美视频一区二区三区-日韩欧美性生活-九九爱这里只有精品-免费av中文字幕在线观看 | 日韩丝袜美女av-日韩av毛片基地-国产精品久久久久久久久kt-久久精品熟女亚洲av蜜臀 | 成人精品久久久免费看一区二区-日韩激情啪啪综合-成人国产av精品免费在线观看-欧美国产黄片在线 精品视频蜜桃久久久久-日韩美免费观看视频-精品99国产乱码久久久久密-久久久久久亚洲女同第一区暖暖 | 国产区一区二区在线观看-欧美日韩中一卡2卡3卡4卡5卡-羞涩色进入亚洲一区二区av-日韩情色精品视频在线 | 国产免看一级a一片成人av-久久99精品久久久久久琪琪-久久中文字幕av-国产av一区二区三区四区最喜欢 | 国产日韩有码中文字幕-99热在线精品自拍-国产一区二区三区蜜桃av-精品乱子伦一区 二区 三区 | julia在线视频中文字幕-五月婷激情四射综合-91成人区人妻精品一区二区三区-hitomi超乳田中瞳中文字幕 | 麻豆www视频在线-中文字幕在线成人精品-91精品国产免费久久久久-久久久精品高清av | 91精品久久综合-激情五月视频网站-东京热日韩av影片-91成年人在线观看 | 亚洲一区二区三区四区五月天-久久人人添人人-超碰日韩97在线-欧美另类少妇熟妇 | 大香蕉大香蕉大香蕉大香蕉-99免费在线观看精品-成人激情在线观看91-激情五月天综合精品 | 激情亚洲精品狠狠操-色婷婷av一区二区三区四区-欧美日韩成人网一区-北条麻妃的av作品在线观看 | 精品丰满熟女少妇一区二区蜜桃-亚洲av欧美av色婷婷伊人-日韩色婷婷中文字幕-超91麻豆精品国产高清在线观看 | 欧美最猛黑人xxxx黑人猛-日韩精品极品视频在-欧美日韩国产精品酒店-变态另类视频一区二区三区 | 麻豆av在线永久免费-欧美激情亚洲精品在线-国产一区二区三区aaaa-综合久久日本久久 | 日本va欧美va亚洲va-久久伊人中文丝袜超碰-国产美女主播av在线免费观看-国产麻豆精品传媒av国产婷婷 | 欧美人妻3p一区二区三-日韩一区二区三区四区高清-久久66热人妻偷产精品9-人妻熟女一区二区三区国产图片 | 成人av亚洲一区二区-亚洲国产精品欧美日韩在线观看-日本中文字幕熟女人妻在线观看-色婷婷亚洲欧洲图片 | 久久久性生活视频-99久久免费国产精品四虎-色婷婷在线视频色婷-日韩小说中文字幕 | 97人人澡人人夜-制服诱惑中文字幕在线观看-91超碰精品日日躁夜夜躁欧美-99精品国产热久久cao三级 | 一区二区三区四区日韩久久-久久精品视频在线看24-国产精品嫩草久久久久久久-日韩精品你懂的视频 亚洲成人av夜夜骚-精品伦一区二区三区视频-日韩欧美p片内射在线观看视频-九九99久久精品在免费线 | 日韩中文字幕福利视频-国产又黄又粗又色又刺激视频-日韩插插插免费视频-久久久久999蜜桃 | 国产中文字幕精品在线观看-国产精品久久88av-久久超逼免费视频-精品老熟妇一区二区三区 | 精品熟妇熟女一区二区三区-中文字幕乱码在线播放视频-人妻少妇中文字幕在线视频-国产中文字幕av网 | 日韩大尺度av在线-成人av在线观看免费网址-久久免费视频观看99-日本精品免费一区二区三区 | 中文字幕av色一区二区三区-乱妇乱女熟妇熟女专区-91康先生在线视频-日韩一区二区三区入口 | 久久日韩美女高清视频视频-在线日韩av一区二区-人人澡人人爽人人射-国产精品99人人爽人人做 | 2020国产自产综合麻豆-日韩欧美国产综合在线一区二区三区-在线亚洲97se亚洲综合在线-骚熟妇av一区二区 |