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Invitrogen™ eIF4H Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA541898

Catalog No. PIPA541898


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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
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