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Rabbit Anti-RUNX1 / AML1 + RUNX3 + RUNX2/AP Conjugated antibody (bs-18598R-AP)
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): 100ul  
100ul/2980.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bs-18598R-AP
英文名稱(chēng)1 Rabbit Anti-RUNX1 / AML1 + RUNX3 + RUNX2/AP Conjugated antibody
中文名稱(chēng) 堿性磷酸酶(AP)標(biāo)記的RUNX1 / AML1 + RUNX3 + RUNX2抗體
別    名 RUNX1_HUMAN; RUNX2_HUMAN; RUNX2_HUMAN.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢(xún)價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng)
產(chǎn)品應(yīng)用 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=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(chǔ) 存 液 Constituents: 0.05M TBS, pH 8.0 with 10mg/ml BSA and 0.05% NaN3, 50% glycerol. Or Lyophilized. Buffer = 0.05M TBS, pH 8.0 with 10mg/ml BSA and 0.05% NaN3. Reconstitute with sterile distilled water.
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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