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Invitrogen™ WBSCR27 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA595711
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
WBSCR27 | |
Polyclonal | |
Unconjugated | |
METTL27 | |
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 | |
Rabbit | |
Affinity Chromatography | |
RUO | |
155368, 688407, 79565 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Immunohistochemistry (Paraffin), Western Blot | |
2.03 mg/mL | |
PBS with 50% glycerol and 0.01% thimerosal; pH 7.3 | |
Q8N6F8 | |
METTL27 | |
Recombinant fusion protein containing a sequence corresponding to amino acids 1-245 of human WBSCR27 (NP_6897722). | |
100 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
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