EIF4H anticorps (C-Term)
Aperçu rapide pour EIF4H anticorps (C-Term) (ABIN2776553)
Antigène
Voir toutes EIF4H AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- C-Term
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Séquence
- TEEERAQRPR LQLKPRTVAT PLNQVANPNS AIFGGARPRE EVVQKEQE
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Homologie
- Cow: 93%, Dog: 93%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 93%, Rat: 100%
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Attributs du produit
- This is a rabbit polyclonal antibody against EIF4H. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the C terminal region of human EIF4H
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
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Commentaires
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Antigen size: 248 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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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 short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))
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Autre désignation
- 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: LNX1, C11orf68, UBC, GINS2, MAT2B, AHSA1, NDRG1, RPS6KA1, PGD, GLA, G6PD, EIF5, EEF2, CASP7, FN1, MRPL44, MRPL9, PUF60, NUDT21, HNRNPA0, SYNCRIP, HNRNPDL, EIF3A, TRA2B, SRSF3, RBMS2, ICT1, EIF4G2, EIF4E, EIF4A1, DGKQ, AI837181,
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
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Pathways
- SARS-CoV-2 Protein Interactome
Antigène
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