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 > Pax-4 Monoclonal Antibody
Pax-4 Monoclonal Antibody
商品貨號(hào)： PLA004979
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： PAX4
  • 蛋白名稱： Paired box protein Pax-4
  • Human_gene_id： 5078
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5078
  • Human_swiss_prot_no： O43316
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/O43316/entry
  • Mouse_swiss_prot_no： P32115
  • Mouse_swiss_link： http://www.uniprot.org/uniprot/P32115
  • 特異性： Pax-4 Monoclonal Antibody detects endogenous levels of Pax-4 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： PAX4; Paired box protein Pax-4
  • 信號(hào)通路： Maturity onset diabetes of the young;
  • 功能： disease:Defects in PAX4 are a cause of noninsulin-dependent diabetes mellitus (NIDDM) [MIM:125853]; also known as diabetes mellitus type 2 or maturity-onset diabetes. NIDDM is characterized by an autosomal dominant mode of inheritance, onset during adulthood and insulin resistance.,disease:Defects in PAX4 are the cause of maturity-onset diabetes of the young type 9 (MODY9) [MIM:612225]. MODY [MIM:606391] is a form of diabetes mellitus characterized by an autosomal dominant mode of inheritance, age of onset of 25 years or younger and a primary defect in insulin secretion.,disease:Genetic variations in PAX4 are associated with susceptibility to insulin-dependent diabetes mellitus (IDDM) [MIM:222100]. IDDM normally starts in childhood or adolescence and is caused by the body's own immune system which destroys the insulin-producing beta cells in the pancreas. Classical features are polydipsia, polyphagia and polyuria, due to hyperglycemia-induced osmotic diuresis.,disease:Genetic variations in PAX4 are associated with susceptibility to ketosis-prone diabetes mellitus (KPD) [MIM:612227]. KPD belongs to a rare subgroup of type 2 diabetes with severe insulin deficiency, mostly observed in subjects of sub-Saharan African ancestry, such as west Africans, Caribbeans and African-Americans. Its phenotype is distinct from the common type 2 and type 1 diabetes. It is characterized by a fulminant initial insulin dependence, without the immunological markers observed in classical type 1 diabetes, followed by a subsequent clinical course which varies from non-insulin treated type 2 diabetes to insulin-dependent idiopathic type 1 diabetes. A severe dysfunction of the insulin-producing beta-cells is attested to by the observation that 25% of the subjects are insulin dependent at diabetes onset, whereas the remaining 75% will develop permanent insulin dependence within 10 years.,function:Plays an important role in the differentiation and development of pancreatic islet beta cells. Transcriptional repressor that binds to a common element in the glucagon, insulin and somatostatin promoters. Competes with PAX6 for this same promoter binding site. The Pax4v isoform appears to be a dominant negative form antagonizing PAX4 transcriptional activity.,sequence caution:According to the human genome assembly there is a stop codon in position 349.,similarity:Belongs to the paired homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,similarity:Contains 1 paired domain.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Nucleus.
  • 組織表達(dá)： Colon,Insulinoma,PCR rescued clones,Placenta,
  • 科研貨號(hào)： PLA004979
Pax-4 Monoclonal Antibody
Catalog No PLA004979
Product information
  • 發(fā)貨日期： 7
  • 基因名稱： PAX4
  • 蛋白名稱： Paired box protein Pax-4
  • Human_gene_id： 5078
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5078
  • Human_swiss_prot_no： O43316
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/O43316/entry
  • Mouse_swiss_prot_no： P32115
  • Mouse_swiss_link： http://www.uniprot.org/uniprot/P32115
  • 特異性： Pax-4 Monoclonal Antibody detects endogenous levels of Pax-4 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： PAX4; Paired box protein Pax-4
  • 信號(hào)通路： Maturity onset diabetes of the young;
  • 功能： disease:Defects in PAX4 are a cause of noninsulin-dependent diabetes mellitus (NIDDM) [MIM:125853]; also known as diabetes mellitus type 2 or maturity-onset diabetes. NIDDM is characterized by an autosomal dominant mode of inheritance, onset during adulthood and insulin resistance.,disease:Defects in PAX4 are the cause of maturity-onset diabetes of the young type 9 (MODY9) [MIM:612225]. MODY [MIM:606391] is a form of diabetes mellitus characterized by an autosomal dominant mode of inheritance, age of onset of 25 years or younger and a primary defect in insulin secretion.,disease:Genetic variations in PAX4 are associated with susceptibility to insulin-dependent diabetes mellitus (IDDM) [MIM:222100]. IDDM normally starts in childhood or adolescence and is caused by the body's own immune system which destroys the insulin-producing beta cells in the pancreas. Classical features are polydipsia, polyphagia and polyuria, due to hyperglycemia-induced osmotic diuresis.,disease:Genetic variations in PAX4 are associated with susceptibility to ketosis-prone diabetes mellitus (KPD) [MIM:612227]. KPD belongs to a rare subgroup of type 2 diabetes with severe insulin deficiency, mostly observed in subjects of sub-Saharan African ancestry, such as west Africans, Caribbeans and African-Americans. Its phenotype is distinct from the common type 2 and type 1 diabetes. It is characterized by a fulminant initial insulin dependence, without the immunological markers observed in classical type 1 diabetes, followed by a subsequent clinical course which varies from non-insulin treated type 2 diabetes to insulin-dependent idiopathic type 1 diabetes. A severe dysfunction of the insulin-producing beta-cells is attested to by the observation that 25% of the subjects are insulin dependent at diabetes onset, whereas the remaining 75% will develop permanent insulin dependence within 10 years.,function:Plays an important role in the differentiation and development of pancreatic islet beta cells. Transcriptional repressor that binds to a common element in the glucagon, insulin and somatostatin promoters. Competes with PAX6 for this same promoter binding site. The Pax4v isoform appears to be a dominant negative form antagonizing PAX4 transcriptional activity.,sequence caution:According to the human genome assembly there is a stop codon in position 349.,similarity:Belongs to the paired homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,similarity:Contains 1 paired domain.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Nucleus.
  • 組織表達(dá)： Colon,Insulinoma,PCR rescued clones,Placenta,
  • 科研貨號(hào)： PLA004979
    • 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

18禁国产麻豆精品久久久久久-超碰人妻av狠狠干-色婷婷综合久久久久久中文-国产av一区二区青青草原 | 99精品视频一区二区三-射射爱天天射天天干天天操-麻豆精品一级片在线观看-亚洲制服人妻另类小说 超碰av中文在线-国产青青操视频在线-在线观看日韩午夜av-精品丰满人妻无套内射 | 97久久久国产精品爽-国产久久久久久久久久一区二区三区四区-99精品视频在线观看视频不卡-久久久精品人妻一区二区三区四 | 国产中文高清视频在线观看-日本中文字幕不卡一二三区-97精品国产91久久久久久久-久久久亚洲熟妇片资源 | 久久精品在线视频播放-蜜桃中文字幕二区-99久久无色码中文字幕人妻-久久精品久久久久久婷婷日 | 91精品aa一区二区三区-九九99热精品国产内外-亚洲精品乱码久久久久久警察-精品久久久中文字幕人 麻豆激情av自拍-另类专区亚洲一区-欧美精品久久99久久久久-丰满熟女人妻一区二区三五十一路 | 日韩av成人一区二区三区-欧美熟妇久久精品-日韩成人在线免费精品视频-久久久精品国产亚洲综合久久久国产 | 美女精品久久久久久久久久久-日本午夜激情插插插-国产成人动漫中文字幕-不卡一卡2卡3卡4卡精品在 | 蜜桃视频在线一区二区-婷婷色六月丁香综合-人妻日本中文字幕在线观看-一级特黄大片欧美久久久蜜臀 | 日韩一卡二卡三卡四卡五卡国产精品视频-99干视频在线观看-一本色道久久88综合日韩精品-99热在线观看完整版 | av成人中文字幕在线观看-久视频中文字幕免费在线精品-国产av系列一区二区-国产一区二区蜜臀大屁股 | 精品人妻中文字幕视频-亚洲成人av新网址-日本精品乱码久久久久-超碰97人人想人人澡 | 婷婷久久五月天丁香-人人妻人人澡人人爽的免费网站-性久久久久久精品一区-国产91精品福利系列 | 风间中文字幕一区二区-亚洲精品自拍第三页-亚洲影院久久久av天天-久久久999免费精品视频 | 999久久久999久久久-国产av天堂一区二区三区-亚洲伊人第一视频一区-亚洲一区二区av手机在线观看 久久国产更新懂色蜜臀-亚洲精品国产成人精品网站-欧美一区两区三区久久-人人妻人人玩操人人 | 中文字幕日韩熟女人妻-人人妻人人插人人爱-huang片网站在线播放-人妻一区二区三区久久夜夜嗨 | 日本久久免费最新区-日韩精品人妻中文字幕有码电影-国产av一区二区三区香蕉-婷婷色婷婷在线观看 久久久在线完整视频-激情四射五月天色-天天天天日天天天天干-麻豆精选在线播放视频 | 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 | 国产视频欧美视频一区二区-久久久久久久久久久久久久久久9-久久er热这里只有精品视频-久久综合亚洲久久另类 | 久久久熟妇色综合激情-天天爽天天操天天做天天干-91麻豆精品国产理论片在线观看-久久热这里都是精品 | 丰满的人妻在线视频-色哟哟网站在线免费-国产精品宾馆性视频-嫩草伊人久久久av少妇 | 婷婷av国产精品推荐-亚洲欧美精品卡一卡二-久久久99人妻一区二区三-91人妻精品国产综合久 | 国产高清精品久久久999-亚洲av国产av手机在线区二-91中文字幕资源网-日韩在线观看视频黑人视频 | 欧美黑人巨大xxxx黑人猛交-91精品国产99久久久久久51-91久久免费在线视频-91国精品产品一区二区三区 | 日韩欧美亚洲一级片-99热精这里只有精品-日韩午夜激情在线观看视频-国产精品久久av在线 | 伊人久久久av老熟妇二区三区-日本国产欧美在线视频一区-国产又粗又黄又硬视频-久久久久精品一区二区三区不卡 | 91麻豆蜜桃在线观看-2021年精品国产福利在线-丁香六月五月婷婷综合-尤物精品在线一区 | 亚洲中文字幕人妻.-日韩在线视频免费播放一区二区-日韩av在线观看电影-少妇人妻精品一区二区三 | 日韩欧美亚洲一级片-99热精这里只有精品-日韩午夜激情在线观看视频-国产精品久久av在线 | 日韩成人激情在线免费观看-97精品国产91久久久久久久厂-日韩欧美一区二区三区视频-日韩啪啪啪中文字幕 | 久久久久精品国产久久-国产麻豆精品**一二三-国产久久草视频在线-91久久精品国产熟女内射 | 麻豆精品在线免费观看视频-久久婷婷六月综合内容-中文字幕视频在线播放-国产亚洲欧洲av一区二区三区 | 亚洲一区二区视频网-嫩草av伊人如意久久-日韩av 一区二区三区四区-久久久中文字幕熟女人妻 | 精品一区二区三区四区五区在线观看-亚洲欧美日韩成人在线激情网-丰满人妻 中文字幕-亚洲五月综合在线婷婷 | 蜜桃视频在线一区二区-婷婷色六月丁香综合-人妻日本中文字幕在线观看-一级特黄大片欧美久久久蜜臀 | 日韩国产毛片在线-av资源 中文字幕-欧美日韩制服丝袜在线-亚洲精品乱码久久久久久97 | www国产精品久久久久久-国产乱子伦一区二区三在线-日韩精品欧美高清-嫩草伊人久久精品少妇蜜桃av | 97久久成人精品视频-久久久久久科技有限公司-蜜臀久久99最新合集-亚洲婷婷一区二区 | 中文字幕一区二区三三-操日本老女人的逼-白木优子中文字幕在线-日韩亚洲免费视频 | 婷婷丁香花综合激情五月天-精品理论一区二区三区-国产成人叼嘿视频在线观看-少妇性视频一区二区 天天操夜夜操狠狠久久-人妻丰满熟妇a v-婷婷中文字幕综合久久-久久国产精品99国产精品72 | 亚洲五月天伊人久久-国产精品久久高潮呻吟无-日韩五十路毛片-91精品久久久久久久久久精 |