產品中(zhōng)心
一抗(kàng)
英文名稱 Anti-C8orf33
中文名稱(chēng) 8號(hào)染(rǎn)色(sè)體開放閱讀(dú)框(kuàng)33抗(kàng)體(tǐ)
別(bié) 名 Chromosome 8 open reading frame 33; Hypothetical protein LOC65265; UPF0488 protein C8orf33;CH033_HUMAN.
詳細(xì)介(jiè)紹：
濃 度(dù) 1mg/1ml
規(guī) 格 0.2ml/200μg
抗體來(lái)源 Rabbit
克隆類(lèi)型 polyclonal
交(jiāo)叉(chā)反(fǎn)應(yīng) Human, Mouse, Rat
產(chǎn)品類(lèi)型(xíng) 一(yī)抗(kàng)
研究(jiū)領域 細胞生物(wù) 免(miǎn)疫學(xué)
蛋白分(fēn)子量(liáng) predicted molecular weight: 25kDa
性(xìng) 狀 Lyophilized or Liquid
免(miǎn) 疫 原(yuán) KLH conjugated synthetic peptide derived from human C8orf33
亞(yà) 型(xíng) IgG
純(chún)化(huà)方(fāng)法(fǎ) affinity purified by Protein A
儲 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產(chǎn)品應用(yòng) WB=1:100-500 ELISA=1:500-1000 IP=1:20-100 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
（石蠟切片需做(zuò)抗原修復(fù)）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保存(cún)條(tiáo)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.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
相關(guān)資(zī)料(liào)：
產(chǎn)品介(jiè)紹 Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf33 gene product has been provisionally designated C8orf33 pending further characterization.
Similarity : Belongs to the UPF0488 family.
Database links : UniProtKB/Swiss-Prot: Q9H7E9.1
