Product Name	Anti-MGAT4A/Cy5.5
Chinese Name	Cy5.5标记的钠/磷酸Transporter1抗体
Alias	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
Research Area	Cell biology The new supersedes the old
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted:Human,Mouse,Rat,Dog,Pig,Horse,Sheep)
Applications	ICC/IF=1:50-200,IF=1:100-500 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Molecular weight	62kDa
Form	Lyophilized or Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human MGAT4A
Lsotype	IgG
Purification	affinity purified by Protein A
Storage Buffer	1M TBS(pH7.4) with 1% BSA, 3% Proclin300 and 50% Glycerol.
Storage	Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 1M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail	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 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 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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