Eukaryotic Translation Initiation Factor 4H (EIF4H) Peptide
EIF4H
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN976261
150,78 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination:
France
Envoi sous 15 à 22 jours ouvrables
Aperçu rapide pour Eukaryotic Translation Initiation Factor 4H (EIF4H) Peptide (ABIN976261)
Antigène
EIF4H
(Eukaryotic Translation Initiation Factor 4H (EIF4H))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-EIF4H antibody (Catalog #: ARP40977_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Purification
- Purified
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))
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Sujet
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EIF4H is 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.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.
Alias Symbols: KIAA0038, WBSCR1, WSCR1, eIF-4H
Protein Interaction Partner: C11orf68,C11orf68
Protein Size: 248 -
Poids moléculaire
- 27 kDa
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ID gène
- 7458
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NCBI Accession
- NM_022170, NP_071496
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UniProt
- Q15056
Antigène
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