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FITC標(biāo)記(jì)的腺(xiàn)苷酸(suān)琥珀(pò)酸(suān)裂解(jiě)酶抗體(tǐ)

文(wén)字(zì):[大][中][小] 2017-5-3    瀏覽(lǎn)次(cì)數:1576    

                                   FITC標記的腺(xiàn)苷(gān)酸琥珀(pò)酸(suān)裂解酶抗(kàng)體                                                                                                                                                
英文名(míng)稱(chēng)Anti-Adenylosuccinate Lyase/FITC
中(zhōng)文(wén)名稱:FITC標記的腺(xiàn)苷酸(suān)琥珀(pò)酸裂解酶抗(kàng)體(tǐ)
別(bié)    名(míng)Adenylosuccinase; Adenylosuccinate lyase; ADSL; AMPS; ASase; ASL; PUR8_HUMAN.  

詳細(xì)介紹:


規格(gé):100ul 
說 明 書(shū)100ul  
研(yán)究領(lǐng)域細胞生物(wù)  信(xìn)號轉導(dǎo)  
抗體來(lái)源Rabbit
克隆(lóng)類(lèi)型(xíng)Polyclonal
交叉反(fǎn)應(yīng) Human, Mouse, Rat, Dog, Pig, Cow, Horse, 
產品應(yīng)用(yòng)IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子(zǐ) 量(liáng)55kDa
性    狀Lyophilized or Liquid
濃(nóng)    度(dù)1mg/ml
免 疫(yì) 原KLH conjugated synthetic peptide derived from human Adenylosuccinate Lyase
亞(yà)    型IgG
純化方法(fǎ)affinity purified by Protein A
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
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.

相(xiāng)關(guān)資料(liào):


產品介紹background:
Adenylsuccinate lyase is involved in both de novo synthesis of purines and formation of adenosine monophosphate from inosine monophosphate. It catalyzes two reactions in AMP biosynthesis: the removal of a fumarate from succinylaminoimidazole carboxamide (SAICA) ribotide to give aminoimidazole carboxamide ribotide (AICA) and removal of fumarate from adenylosuccinate to give AMP. Adenylosuccinase deficiency results in succinylpurinemic autism, psychomotor retardation, and , in some cases, growth retardation associated with muscle wasting and epilepsy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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