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Rabbit Anti-MGAT4A  antibody (bs-18907R)  
~~~促銷代碼KT202411~~~
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說明書: 50ul  100ul  200ul
50ul/1180.00元
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200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號 bs-18907R
英文名稱 Rabbit Anti-MGAT4A  antibody
中文名稱 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  
Specific References  (1)     |     bs-18907R has been referenced in 1 publications.
[IF=1.664] Zhang PF et al. MicroRNA-139 suppresses hepatocellular carcinoma cell proliferation and migration by directly targeting Topoisomerase I. ONCOLOGY LETTERS 17: 1903-1913, 2019  WB ;  Human.  
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,Pig,Sheep,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 62kDa
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MGAT4A: 431-535/535 
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 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.

SWISS:
Q14916

Gene ID:
6568

Database links:

Entrez Gene: 6568 Human

Entrez Gene: 20504 Mouse

Entrez Gene: 171080 Rat

Omim: 182308 Human

SwissProt: Q14916 Human

SwissProt: Q61983 Mouse

SwissProt: Q62795 Rat

Unigene: 205816 Human

Unigene: 2656 Mouse

Unigene: 11150 Rat



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