| 產(chǎn)品編號(hào) | bs-16195R |
| 英文名稱(chēng) | Rabbit Anti-FUNDC2 antibody |
| 中文名稱(chēng) | Cervical cancer oncogene 3/宮頸癌原癌基因3抗體 |
| 別 名 | Cervical cancer oncogene 3; Cervical cancer proto oncogene 3 protein; DC44; FLJ33773; FUN14 domain containing 2; FUN14 domain containing protein 2; FUNDC 2; HCBP 6; HCBP6; FUND2_HUMAN; HCC 3; HCC3; Hepatitis C virus core binding protein 6; MGC131676; MGC2495; OTTHUMP00000015441; OTTHUMP00000061459; PD03104. |
| 研究領(lǐng)域 | 腫瘤 細(xì)胞生物 轉(zhuǎn)錄調(diào)節(jié)因子 細(xì)菌及病毒 新陳代謝 線粒體 表觀遺傳學(xué) |
| 抗體來(lái)源 | Rabbit |
| 克隆類(lèi)型 | Polyclonal |
| 交叉反應(yīng) | (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,Horse) |
| 產(chǎn)品應(yīng)用 | IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 21kDa |
| 細(xì)胞定位 | 細(xì)胞核 細(xì)胞漿 線粒體 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human FUNDC2: 101-189/189 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 產(chǎn)品介紹 |
FUNDC2 is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. Function: The function of FUNDC2 (FUN14 domain-containing protein 2) is unknown. Subcellular Location: Mitochondrial Similarity: Belongs to the FUN14 family. SWISS: Q9BWH2 Gene ID: 65991 Database links: Entrez Gene: 65991 Human Entrez Gene: 67391 Mouse SwissProt: Q9BWH2 Human SwissProt: Q9D6K8 Mouse Unigene: 356050 Human Unigene: 126404 Mouse |
