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|Tested species reactivity||Mouse, Rat|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Recombinant fragment corresponding to a region within amino acids 131 and 849 of MGEA5|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS, pH 7, with 20% glycerol|
|Storage Conditions||-20° C, Avoid Freeze/Thaw Cycles|
|Tested Applications||Dilution *|
|Immunohistochemistry (Paraffin) (IHC (P))||1:100-1:1000|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
The dynamic modification of cytoplasmic and nuclear proteins by O-linked N-acetylglucosamine (O-GlcNAc) addition and removal on serine and threonine residues is catalyzed by OGT (MIM 300255), which adds O-GlcNAc, and MGEA5, a glycosidase that removes O-GlcNAc modifications (Gao et al., 2001 [PubMed 11148210]). [supplied by OMIM].
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Beta-hexosaminidase; Beta-N-acetylhexosaminidase; Bifunctional protein NCOAT; MEA5; meningioma expressed antigen 5 hyaluronidase; Meningioma-expressed antigen 5; N-acetyl-beta-D-glucosaminidase; N-acetyl-beta-glucosaminidase; nuclear cytoplasmic O-GlcNAcase and acetyltransferase; OGA; Protein O-GlcNAcase
2810009A20Rik; 4833427O07Rik; 5830447M11Rik; AA408215; Hexc; Hy5; Kiaa0679; Mea5; Mgea5; mKIAA0679; Ncoat; O-GLCNACASE; OGA