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泛素激活酶E1抗體

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產(chǎn)品名稱: 泛素激活酶E1抗體
產(chǎn)品型號(hào): E1 Ubiquitin Activating Enzyme
產(chǎn)品展商: 單克隆抗體/多克隆抗體
產(chǎn)品文檔: 無相關(guān)文檔

簡單介紹

泛素激活酶E1抗體應(yīng)用于IHC、WB、 IF、IP、ELISA等科研實(shí)驗(yàn),按理化性質(zhì)和生物學(xué)功能IgM、IgG、IgA、IgE、IgD五類。按抗體的來源,可將其分為天然抗體和**抗體。泛素激活酶E1抗體生產(chǎn)每個(gè)流程都執(zhí)行嚴(yán)格的檢測標(biāo)準(zhǔn),保證蛋白抗原產(chǎn)品質(zhì)量,質(zhì)量穩(wěn)定,實(shí)驗(yàn)效果明顯。


泛素激活酶E1抗體  的詳細(xì)介紹

泛素激活酶E1抗體

規(guī)格:1mg/1ml

英文名: E1 Ubiquitin Activating Enzyme

別名: A1S9; A1S9 protein; A1S9T and BN75 temperature sensitivity complementing; A1S9T; A1ST; GXP 1; GXP1; MGC4781; Protein A1S9; Uba1; UBA1_HUMAN; UBE 1 ; UBE 1X; UBE1; UBE1X; Ubiquitin activating enzyme E1

分子量: 118kDa

儲(chǔ)存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆類型:Polyclonal

亞型:IgG

純化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human UBE1

交叉反應(yīng):Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep,

細(xì)胞定位:

泛素激活酶E1抗體產(chǎn)品介紹:background: The protein encoded by this gene catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation. This gene complements an X-linked mouse temperature-sensitive defect in DNA synthesis, and thus may function in DNA repair. It is part of a gene cluster on chromosome Xp11.23. Alternatively spliced transcript variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]. Function: Activates ubiquitin by first adenylating its C-terminal glycine residue with ATP, and thereafter linking this residue to the side chain of a cysteine residue in E1, yielding an ubiquitin-E1 thioester and free AMP. Subunit: Monomer (By similarity). Interacts with GAN (via BTB domain). Post-translational modifications: ISGylated. DISEASE: Defects in UBA1 are the cause of spinal muscular atrophy X-linked type 2 (SMAX2) [MIM:301830]; also known as X-linked lethal infantile spinal muscular atrophy, distal X-linked arthrogryposis multiplex 泛素激活酶E1抗體congenita or X-linked arthrogryposis type 1 (AMCX1). Spinal muscular atrophy refers to a group of neuromuscular disorders characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy. SMAX2 is a lethal infantile form presenting with hypotonia, areflexia, and multiple congenital contractures. Similarity: Belongs to the ubiquitin-activating E1 family. Gene ID: 7317 Database links: Entrez Gene: 7317 Human Entrez Gene: 22201 Mouse Entrez Gene: 314432 Rat Omim: 314370 Human SwissProt: 泛素激活酶E1抗體P22314 Human SwissProt: Q02053 Mouse SwissProt: Q5U300 Rat Unigene: 533273 Human Unigene: 1104 Mouse Unigene: 474674 Mouse Unigene: 11800 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

泛素激活酶E1抗體產(chǎn)品應(yīng)用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù)) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究領(lǐng)域:細(xì)胞生物  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  表觀遺傳學(xué)  

儲(chǔ)存條件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

來源: Rabbit

外觀: Lyophilized or Liquid




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