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Invitrogen™ eIF4H Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA541898
Description
Peptide sequence: DSRDDFNSGF RDDFLGGRGG SRPGDRRTGP PMGSRFRDGP PLRGSNMDFR Sequence homology: Dog: 100%; Horse: 86%; Human: 100%; Mouse: 93%; Pig: 100%; Rat: 93%.
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
Specifications
eIF4H | |
Polyclonal | |
Unconjugated | |
EIF4H | |
AU018978; D5Ertd355e; E430026L18Rik; Ef4h; EIF4H; eIF-4H; Eukaryotic translation initiation factor 4H; KIAA0038; mKIAA0038; WBSCR1; Williams-Beuren syndrome chromosomal region 1 protein; Williams-Beuren syndrome chromosomal region 1 protein homolog; Williams-Beuren syndrome chromosome region 1; Williams-Beuren syndrome chromosome region 1 homolog; WSCR1 | |
Rabbit | |
Protein A | |
RUO | |
7458 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
1 mg/mL | |
PBS with 2% sucrose and 0.09% sodium azide | |
Q15056 | |
EIF4H | |
Synthetic peptide directed towards the middle region of human WBSCR1. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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