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Invitrogen™ WBSCR27 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA595711

Catalog No. PIPA595711


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Description

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].
TRUSTED_SUSTAINABILITY
Specifications

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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