索引：食道癌相關(guān)基因4蛋白抗體科研實(shí)驗(yàn)使用

中文名稱    食道癌相關(guān)基因4蛋白抗體    

英文名稱    ECRG4    

別    名    AUGN_HUMAN; Augurin; C2orf40; Esophageal cancer-related gene 4 protein.    

供 應(yīng) 商    遠(yuǎn)慕生物

研究領(lǐng)域    腫瘤  細(xì)胞生物  神經(jīng)生物學(xué)  生長(zhǎng)因子和激素      

抗體來(lái)源    Rabbit    

克隆類型    Polyclonal    

交叉反應(yīng)    Human, Mouse, Rat, Dog, Pig, Rabbit,     

產(chǎn)品應(yīng)用    WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1:20-100 IF=1:50-200 IEM=1:20-200 IGS=1:20-200 GICA=1:20-200 食道癌相關(guān)基因4蛋白抗體（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.    

分 子 量    7.8kDa    

細(xì)胞定位    細(xì)胞漿 分泌型蛋白     

性    狀    Lyophilized or Liquid    

濃    度    1mg/1ml    

免 疫 原    KLH conjugated synthetic peptide derived from human ECRG4/C2orf40    

亞    型    IgG    

純化方法    affinity purified by Protein A    

儲(chǔ) 存 液    Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4    

保存條件    Store at -20 癈 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癈. 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 癈.    

食道癌相關(guān)基因4蛋白抗體產(chǎn)品介紹    background:

ECRG4, also known as augurin or C2orf40, is a 148 amino acid secreted protein. Belonging to the augurin family, ECRG4 is thought to be a hormone. It has also been suggested that ECRG4 may act as a tumor suppressor. The gene that encodes ECRG4 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes.

Function:
Probable hormone that may induce senescence of oligodendrocyte and neural precursor cells, characterized by G1 arrest, RB1 dephosphorylation and accelerated CCND1 and CCND3 proteasomal degradation.

Subcellular Location:
Secreted. Cytoplasmic vesicle, secretory vesicle.

Similarity:
Belongs to the augurin family.

Database links:

Entrez Gene: 84417 Human

Omim: 611752 Human

SwissProt: Q9H1Z8 Human

Unigene: 43125 Human


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