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 > 抗體 > 一抗 > 其它 > PLZF Monoclonal Antibody
PLZF Monoclonal Antibody
商品貨號： PLA004993
適 應(yīng) 性： 人
WB IF ELISA
￥600元
規(guī)格：
在線咨詢
MSDS
說明書
商品描述
  • 發(fā)貨日期： 7
  • 基因名稱： ZBTB16
  • 蛋白名稱： Zinc finger and BTB domain-containing protein 16
  • Human_gene_id： 7704
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=7704
  • Human_swiss_prot_no： Q05516
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/Q05516/entry
  • 特異性： PLZF Monoclonal Antibody detects endogenous levels of PLZF protein.
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源： Monoclonal, Mouse
  • 稀釋： WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.
  • 純化工藝： Affinity purification
  • 儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書： 1
  • Msds： MSDS_Antibody.pdf
  • 其他名稱： ZBTB16; PLZF; ZNF145; Zinc finger and BTB domain-containing protein 16; Promyelocytic leukemia zinc finger protein; Zinc finger protein 145; Zinc finger protein PLZF
  • 信號通路： Pathways in cancer;Acute myeloid leukemia;
  • 功能： disease:A chromosomal aberration involving ZBTB16 may be a cause of acute promyelocytic leukemia (APL). Translocation t(11;17)(q32;q21) with RARA.,disease:Defects in ZBTB16 are the cause of skeletal defects genital hypoplasia and mental retardation [MIM:612447]. The disorder is characterized by mental retardation, craniofacial dysmorphism, microcephaly and short stature. Additional features include absence of the thumbs, hypoplasia of the radii and ulnae, additional vertebrae and ribs, retarded bone age and genital hypoplasia.,function:Probable transcription factor. May play a role in myeloid maturation and in the development and/or maintenance of other differentiated tissues. Probable substrate-recognition component of an E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.,induction:By retinoic acid.,pathway:Protein modification; protein ubiquitination.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family.,similarity:Contains 1 BTB (POZ) domain.,similarity:Contains 9 C2H2-type zinc fingers.,subunit:Binds EPN1. Interacts with ZBTB32 and CUL3.,tissue specificity:Within the hematopoietic system, PLZF is expressed in bone marrow, early myeloid cell lines and peripheral blood mononuclear cells. Also expressed in the ovary, and at lower levels, in the kidney and lung.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細胞定位： Nucleus . Nucleus, nuclear body .
  • 組織表達： Within the hematopoietic system, PLZF is expressed in bone marrow, early myeloid cell lines and peripheral blood mononuclear cells. Also expressed in the ovary, and at lower levels, in the kidney and lung.
  • 科研貨號： PLA004993
PLZF Monoclonal Antibody
Catalog No PLA004993
Product information
  • 發(fā)貨日期： 7
  • 基因名稱： ZBTB16
  • 蛋白名稱： Zinc finger and BTB domain-containing protein 16
  • Human_gene_id： 7704
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=7704
  • Human_swiss_prot_no： Q05516
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/Q05516/entry
  • 特異性： PLZF Monoclonal Antibody detects endogenous levels of PLZF protein.
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源： Monoclonal, Mouse
  • 稀釋： WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.
  • 純化工藝： Affinity purification
  • 儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書： 1
  • Msds： MSDS_Antibody.pdf
  • 其他名稱： ZBTB16; PLZF; ZNF145; Zinc finger and BTB domain-containing protein 16; Promyelocytic leukemia zinc finger protein; Zinc finger protein 145; Zinc finger protein PLZF
  • 信號通路： Pathways in cancer;Acute myeloid leukemia;
  • 功能： disease:A chromosomal aberration involving ZBTB16 may be a cause of acute promyelocytic leukemia (APL). Translocation t(11;17)(q32;q21) with RARA.,disease:Defects in ZBTB16 are the cause of skeletal defects genital hypoplasia and mental retardation [MIM:612447]. The disorder is characterized by mental retardation, craniofacial dysmorphism, microcephaly and short stature. Additional features include absence of the thumbs, hypoplasia of the radii and ulnae, additional vertebrae and ribs, retarded bone age and genital hypoplasia.,function:Probable transcription factor. May play a role in myeloid maturation and in the development and/or maintenance of other differentiated tissues. Probable substrate-recognition component of an E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.,induction:By retinoic acid.,pathway:Protein modification; protein ubiquitination.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family.,similarity:Contains 1 BTB (POZ) domain.,similarity:Contains 9 C2H2-type zinc fingers.,subunit:Binds EPN1. Interacts with ZBTB32 and CUL3.,tissue specificity:Within the hematopoietic system, PLZF is expressed in bone marrow, early myeloid cell lines and peripheral blood mononuclear cells. Also expressed in the ovary, and at lower levels, in the kidney and lung.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細胞定位： Nucleus . Nucleus, nuclear body .
  • 組織表達： Within the hematopoietic system, PLZF is expressed in bone marrow, early myeloid cell lines and peripheral blood mononuclear cells. Also expressed in the ovary, and at lower levels, in the kidney and lung.
  • 科研貨號： PLA004993
    • 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.
普拉特澤實驗室電話助手

4006916686

掃碼咨詢

麻豆一级黄色大片-亚洲图片,偷拍自拍区-日韩精品在线免费观看高清视频-久操免费福利资源站 | 欧美日韩一级久久久-999精品丰满人妻少妇-婷婷爱亚洲中文字幕-日韩午夜精品二 | 91精品国产99久久久久久-中文字幕国产精品麻豆-激情五月天色婷婷网-欧美 另类 激情 亚洲 | av中文字幕在线观看在线-久久久久精品国产乱码78m-国产麻豆剧传媒精品国产av吴梦-69中文字幕一区二区三区 | 久热在线中文免费视频-少妇啪啪av一区二区三区-高清一区二区三区四区免费视频-人妻少妇精品中文字幕专区视频 | 开心激情五月天在线视频观看-久久久久999国产精品-国产又粗又黄又猛的视频-伊人网伊人网伊人网伊人网 | 麻豆精品一区二区观看-日韩午夜久久久久久久久久-亚洲天堂中文字幕网-日本精品一区二区三区不卡 色综合久久久久综合一小说-91福利视频下载-一本色道久久综合狠狠躁最新章节-999国产精品亚洲7777 | 日韩制服丝袜在线播放-嫩草精产一二三产区-久久这里只有精品视频3-国产精品成人三级在线观看 | 国产精品永久免费av在线怀-中文字幕高清成人三级-9久久99热这里只有精品-国产精品久久久久久精品小说 | av麻豆电影网址撸-国产精品久久久免费av-特黄特色毛片免费看-亚洲男人av天堂吧 | 欧美不卡一区二区视频-欧美 日韩 国产 第一页-日本va欧美va欧美va-日韩欧美一区二区三区在线 | 日韩美女免费视频啪-17c视频在线观看一区二区-久热这里只有精品9-18岁日韩内射颜射午夜久久成人 9久久婷婷国产综合精品性色-日韩日韩日韩日韩日韩日韩av-99久久亚洲精品婷婷-日韩激情中文字幕视频 | 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 | av日韩毛片免费看-国产av1区,二区,三区-天天干天天日天天操天天干-婷婷中文字幕4 | 国产乱淫av一区二区三区-久久国产精久久精产国-日韩,亚洲高清不卡-2020中文字幕在线视频一区 | 99精品视频a级视频在线观看-日本又黄又爽的视频-久久国产 中文字幕-久久久亚洲综合视频 | 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 | 国产黄色小视频看看-久久大久久就久久精品欧美-日韩精品视频在线免费观看首页-国产麻豆精品视频网 | 久久久www免费人成精品-国产精品久久久精品三级ar↗-国产偷自视频区视频一区二区-九九久久久久婷婷 | 久久亚洲av西西人体-伊人久久av丝袜综合-久久久一区二区三区视频不卡-99国产精品视频久久久久 | 亚洲av极品精品在线观看-亚洲综合久久久蜜桃-你懂的中文字幕-激情深爱亚洲综合久久 | 麻豆回家视频一二三-日韩黄色av在线观看-国产又大又黄又爽的视频-麻豆免费视频传媒 | 中文字幕成人亚洲精品-久久精品国产亚洲a∨成人-日韩有码免费在线观看视频-久久中文字幕亚洲精品最新 | 99热这里只有精品2019-国产最新视频一区二区-久久精品亚洲美女-日韩av尤物丰满一区二区 | 人妻中文字幕乱码系列-懂色av一区二区三区网久久-亚洲欧洲日韩第一区-在线人成免费视频97国产 | 在线观看国产成人99-成年女人毛片免费观看不卡-亚洲人妻一区中出-日韩人妻精品免费视频 | 1024欧美日韩精品久久久-黑人爆操日本女-青青久久免费一区二区视频-国产精品88久久久久久妇女 | 日韩av一区在线免费观看-亚洲日本一区二区三区不卡-日韩 欧美 综合 一区-日韩不卡激情网站 | 亚洲天堂男人网亚洲天堂女人网-亚洲精品久久中文字幕xx-久久久久久久精美人妻-国产激情黑人91蜜 天天操天天干天天日天天操-人妻少妇久久久一区二区三区-日韩男女三级视频-国产又粗又猛又爽又黄的黄牛视频 | 精品一区二区视频一-国产人妖一区二区av-日韩变态深喉口爆图片-国产乱色乱子伦一区二区三区 | 精品99在线免费视频-婷婷伊人综合一区-日韩免费在线观看毛片网站-久久亚洲精品国产av | 久久躁夜夜躁日日躁-精品99视频播放在线观看-欧洲日韩视频一区二区三区-天天射天天操天天操 | 日韩成人a电影免费-国产一区二区三区男人吃奶-激情五月色婷婷综合-久久精品一区二区中文字幕 | 亚洲视频区自拍高清-精品国产乱码久久久久久中文-91在线中文字幕在线观看-国产又大又黄又硬又爽 国产 日韩 欧美片-中文字幕日韩av在线-一本色道88久久加勒比-伦中文字幕自拍偷拍热久av | 欧美一区二区三区免费不卡视频-亚洲欧美情色在线观看-久久久久精品人妻一区-国产91亚洲精品久久久久 | 日韩激情欧美激情-国产 日韩 欧美 综合-激情五月天最新视频网址-欧美精选一区二区三区四区 | 国产成人va网站在线观看-91久久偷拍我视频-国产aaa精品视频-91大神久久久久久久久久 | 日本精品一区二区三区别区-亚洲欧美日韩中文字幕一区二区-蜜桃久久精品在线-久久久久精品久久久水蜜桃导演 | 97超碰中文字幕总站-欧美精品熟妇视频-蜜桃av鲁一鲁一鲁一鲁一区二区三区-日韩情色偷拍自拍 | 国产精品亚洲精品日韩已满十八小-丰满人妻一区二区三区免费看-91日韩中文字幕在线视频-年轻的母亲中文字幕在线看 | 久久青青草原av国产-国产熟女一区二区三区五月婷小说-五月婷婷综合激情网-国产91精品久久久久久一级 |