missing translation for 'onlineSavingsMsg'
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Invitrogen™ WBSCR27 Polyclonal Antibody

Description
Immunogen sequence: MAQEEGGSLP EVRARVRAAH GIPDLAQKLH FYDRWAPDYD QDVATLLYRA PRLAVDCLTQ ALPGPPHSAL ILDVACGTGL VAAELRAPGF LQLHGVDGSP GMLEQAQAPG LYQRLSLCTL GQEPLPSPEG TFDAVLIVGA LSDGQVPCNA IPELHVTKPG GLVCLTTRTN SSNLQYKEAL EATLDRLEQA GMWEGLVAWP VDRLWTAGSW LPPSWRWYPA SLPRMASSPA LSTCTESGRR PRLRK; Positive Samples: HT-29, MCF7, Mouse lung.
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008].
Specifications
Specifications
| Antigen | WBSCR27 |
| Applications | ELISA, Immunohistochemistry (Paraffin), Western Blot |
| Classification | Polyclonal |
| Concentration | 2.03 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.01% thimerosal; pH 7.3 |
| Gene | METTL27 |
| Gene Accession No. | Q8N6F8 |
| Gene Alias | AW492986; BC002286; Methyltransferase-like protein 27; METTL27; WBSCR27; Williams Beuren syndrome chromosome region 27; Williams Beuren syndrome chromosome region 27 (human); Williams-Beuren syndrome chromosomal region 27 protein; Williams-Beuren syndrome chromosome region 27 homolog |
| Gene Symbols | METTL27 |
| Show More |
Product Title
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