EIF4H polyclonal antibody
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More Files
- More Functions
Western Blot (Cell lysate)
Western Blot analysis of Jurkat cell lysate with EIF4H polyclonal antibody (Cat # PAB30048) at 2.5 ug/mL working concentration.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with EIF4H polyclonal antibody (Cat # PAB30048) at 4-8 ug/mL working concentration.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of human EIF4H.
Immunogen
A synthetic peptide corresponding to internal region of human EIF4H.
Sequence
DSRDDFNSGFRDDFLGGRGGSRPGDRRTGPPMGSRFRDGPPLRGSNMDFR
Host
Rabbit
Theoretical MW (kDa)
27
Reactivity
Human
Form
Liquid
Purification
Protein A purification
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (4-8 ug/mL)
Western Blot (2.5 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (2% sucrose, 0.09% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western Blot analysis of Jurkat cell lysate with EIF4H polyclonal antibody (Cat # PAB30048) at 2.5 ug/mL working concentration.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with EIF4H polyclonal antibody (Cat # PAB30048) at 4-8 ug/mL working concentration. -
Gene Info — EIF4H
Entrez GeneID
7458GeneBank Accession#
NM_022170Protein Accession#
NP_071496;Q15056Gene Name
EIF4H
Gene Alias
KIAA0038, WBSCR1, WSCR1
Gene Description
eukaryotic translation initiation factor 4H
Omim ID
603431Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
OTTHUMP00000024643|Williams-Beuren syndrome chromosome region 1
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Interactome
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Disease
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