| 產(chǎn)品編號 | bs-18633R-Gold |
| 英文名稱1 | Rabbit Anti-MAGT1/Gold Conjugated antibody |
| 中文名稱 | 膠體金標(biāo)記的鎂轉(zhuǎn)運(yùn)蛋白1抗體 |
| 別 名 | bA217H1; DKFZp564K142; FLJ14726; IAG2; IAP; Implantation-associated protein; Magnesium transporter 1; MagT1; MGC64926; MRX95; Oligosaccharyltransferase 3 homolog B; OST3B; OTTHUMP00000023589; OTTHUMP00000062081; PRO0756; RP11-217H1.1. |
| 規(guī)格價(jià)格 | 100ul/2980元 購買 大包裝/詢價(jià) |
| 說 明 書 | 100ul（10nm 15nm 35nm） |
| 研究領(lǐng)域 | 細(xì)胞生物 結(jié)合蛋白 |
| 抗體來源 | Rabbit |
| 克隆類型 | Polyclonal |
| 交叉反應(yīng) | Mouse, Rat, (predicted: Human, Dog, Pig, Cow, Horse, Rabbit, Sheep, ) |
| 產(chǎn)品應(yīng)用 | IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 35kDa |
| 性 狀 | Lyophilized or Liquid |
| 濃 度 | 0.4mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human MAGT1 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 儲 存 液 | 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300. |
| 保存條件 | Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles. |
| 產(chǎn)品介紹 |
background: This gene encodes a magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause mental retardation X-linked type 95 (MRX95). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jan 2010] Function: May be involved in N-glycosylation through its association with N-oligosaccharyl transferase. May be involved in Mg2+ transport in epithelial cells. Subunit: Weakly associates with the oligosaccharyl transferase (OST) complex which contains at least RPN1/ribophorin I, RPN2/ribophorin II, OST48, DAD1, and either STT3A or STT3B Subcellular Location: Cell membrane. Tissue Specificity: Ubiquitous. Expressed at very low levels in brain, lung and kidney. DISEASE: Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia (XMEN) [MIM:300853]: A disease characterized by CD4 lymphopenia, severe chronic viral infections, and defective T-lymphocyte activation. Note: The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the OST3/OST6 family. Contains 1 thioredoxin domain. Database links: Entrez Gene: 84061 Human Entrez Gene: 67075 Mouse Omim: 300715 Human SwissProt: Q9H0U3 Human SwissProt: Q9CQY5 Mouse Unigene: 323562 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
