| 產(chǎn)品編號 | bs-18907R-Gold |
| 英文名稱 | Rabbit Anti-MGAT4A/Gold Conjugated antibody |
| 中文名稱 | 膠體金標(biāo)記的鈉/磷酸轉(zhuǎn)運(yùn)蛋白1抗體 |
| 別 名 | Alpha 1 3 mannosyl glycoprotein 4 beta N acetylglucosaminyltransferase A; Alpha 1 3 mannosyl glycoprotein beta 1 4 N acetylglucosaminyltransferase; GlcNAc T IVa; GNT IV; GNT IVA; MGT4A_HUMAN; GNTIV; GNTIVA; Mannosyl (alpha 1 3 ) glycoprotein beta 1 4 N acetylglucosaminyltransferase isoenzyme A; Mannosyl (alpha 1,3) glycoprotein beta 1,4 N acetylglucosaminyltransferase; MGAT 4A; N acetylglucosaminyltransferase IVa; N glycosyl oligosaccharide glycoprotein N acetylglucosaminyltransferase IVa; Na(+)/PI cotransporter 1; Na/Pi-4; Renal Na(+)-dependent phosphate cotransporter 1; Renal sodium-dependent phosphate transport protein 1; Sodium-dependent phosphate transport protein 1; Sodium/phosphate cotransporter 1; UDP GlcNAc:a 1 3 D mannoside b 1 4 acetylglucosaminyltransferase IV; UDP N acetylglucosamine: alpha 1 3 D mannoside beta 1 4 N acetylglucosaminyltransferase IVa; UDP N acetylglucosamine:alpha1 3 d mannoside beta1 4 N acetylglucosaminyltransferase |
| 規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
| 說 明 書 | 100ul（10nm 15nm 35nm） |
| 研究領(lǐng)域 | 細(xì)胞生物 新陳代謝 |
| 抗體來源 | Rabbit |
| 克隆類型 | Polyclonal |
| 交叉反應(yīng) | (predicted: Human, Mouse, Rat, Dog, Pig, Horse, 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 | 62kDa |
| 性 狀 | Lyophilized or Liquid |
| 濃 度 | 0.4mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human MGAT4A |
| 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: MFSD8 is a 518 amino acid multi-pass membrane protein of the lysosome that is thought to function as a carrier protein that transports small solutes by way of chemiosmotic ion gradients. Expressed at low levels in many tissues, MFSD8 is encoded by a gene that maps to human chromosome 4q28.1. Defects in the gene encoding MFSD8 are the cause of a late infantile neuronal ceroid lipofuscinosis known as neuronal ceroid lipofuscinosis type 7 (CLN7). CLN7 is characterized by seizures, progressive dementia and visual failure. Function: May be a carrier that transport small solutes by using chemiosmotic ion gradients Subcellular Location: Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A soluble form: Secreted (By similarity). Tissue Specificity: Expressed at very low levels in all tissues tested. Similarity: Belongs to the glycosyltransferase 54 family. Database links: Entrez Gene: 6568 Human Entrez Gene: 20504 Mouse Omim: 182308 Human SwissProt: Q14916 Human SwissProt: Q61983 Mouse Unigene: 205816 Human Unigene: 2656 Mouse Unigene: 11150 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
