產(chǎn)品編號 | bs-20081R |
英文名稱 | FAM5B Rabbit pAb |
中文名稱 | FAM5B蛋白抗體 |
別 名 | BMP/retinoic acid-inducible neural-specific protein 2; DBCCR1-like protein 2; Fam5b; BRNP2_HUMAN; Protein FAM5B. |
研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
克 隆 號 | |
交叉反應(yīng) | (predicted: Human) |
產(chǎn)品應(yīng)用 | 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 | 85 kDa |
檢測分子量 | |
細(xì)胞定位 | 細(xì)胞漿 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human FAM5B: 331-430/784 |
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 | 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 |
BRINP2 is a 783 amino acid secreted protein that belongs to the FAM5 family. Existing as two alternatively spliced isoforms, BRINP2 is encoded by a gene that maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma. Subcellular Location: Secreted. Similarity: Belongs to the FAM5 family. Contains 1 MACPF domain. SWISS: Q9C0B6 Gene ID: 57795 Database links: Entrez Gene: 57795 Human Entrez Gene: 240843 Mouse SwissProt: Q9C0B6 Human SwissProt: Q6DFY8 Mouse Unigene: 495918 Human Unigene: 329579 Mouse Unigene: 22596 Rat |