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            Rabbit Anti-RUNX1 / AML1 + RUNX3 + RUNX2/Cy5.5 Conjugated antibody (bs-18598R-Cy5.5)
            訂購熱線:400-901-9800
            訂購郵箱:sales@m.p2b3.cn
            訂購QQ:  400-901-9800
            技術(shù)支持:techsupport@m.p2b3.cn
            說 明 書: 100ul  
            100ul/2980.00元
            大包裝/詢價
            產(chǎn)品編號 bs-18598R-Cy5.5
            英文名稱 Rabbit Anti-RUNX1 / AML1 + RUNX3 + RUNX2/Cy5.5 Conjugated antibody
            中文名稱 Cy5.5標(biāo)記的RUNX1 / AML1 + RUNX3 + RUNX2抗體
            別    名 RUNX1_HUMAN; RUNX2_HUMAN; RUNX2_HUMAN.  
            規(guī)格價格 100ul/2980元 購買        大包裝/詢價
            說 明 書 100ul  
            研究領(lǐng)域
            抗體來源 Rabbit
            克隆類型 Polyclonal
            交叉反應(yīng)
            產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
            not yet tested in other applications.
            optimal dilutions/concentrations should be determined by the end user.
            分 子 量 45-57kDa
            性    狀 Lyophilized or Liquid
            濃    度 1mg/ml
            免 疫 原 KLH conjugated synthetic peptide derived from human RUNX1 / AML1 + RUNX3 + RUNX2
            亞    型 IgG
            純化方法 affinity purified by Protein A
            儲 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4.
            保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
            產(chǎn)品介紹 background:
            This gene is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing. [provided by RefSeq, Jul 2008]

            Database links:

            Entrez Gene: 860 Human

            Entrez Gene: 861 Human

            Entrez Gene: 864 Human

            Entrez Gene: 12393 Mouse

            Entrez Gene: 12394 Mouse

            Entrez Gene: 12399 Mouse

            Entrez Gene: 156726 Rat

            Entrez Gene: 367218 Rat

            Entrez Gene: 50662 Rat

            Omim: 151385 Human

            Omim: 600210 Human

            Omim: 600211 Human

            SwissProt: Q01196 Human

            SwissProt: Q13761 Human

            SwissProt: Q13950 Human

            SwissProt: Q03347 Mouse

            SwissProt: Q08775 Mouse

            SwissProt: Q64131 Mouse

            SwissProt: Q63046 Rat

            SwissProt: Q9Z2J9 Rat

            Unigene: 149261 Human

            Unigene: 170019 Human

            Unigene: 535845 Human

            Unigene: 612648 Human

            Unigene: 378894 Mouse

            Unigene: 391013 Mouse

            Unigene: 391017 Mouse

            Unigene: 4081 Mouse

            Unigene: 470227 Mouse

            Unigene: 11201 Rat

            Unigene: 214214 Rat

            Unigene: 34220 Rat

            Unigene: 83672 Rat



            Important Note:
            This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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