Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1) Peptide
EEF1A1
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN976145
Aperçu rapide pour Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1) Peptide (ABIN976145)
Antigène
eEF1A1 (EEF1A1)
(Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1))
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-EEF1A1 antibody (Catalog #: ARP48166_T100). 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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- eEF1A1 (EEF1A1) (Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1))
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Sujet
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EEF1A1 is an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas, and the other isoform (alpha 2) is expressed in brain, heart and skeletal muscle. This isoform is identified as an autoantigen in 66 % of patients with Felty syndrome.This gene encodes an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas, and the other isoform (alpha 2) is expressed in brain, heart and skeletal muscle. This isoform is identified as an autoantigen in 66 % of patients with Felty syndrome. This gene has been found to have multiple copies on many chromosomes, some of which, if not all, represent different pseudogenes. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: CCS-3, CCS3, EEF-1, EEF1A, EF-Tu, EF1A, FLJ25721, GRAF-1EF, HNGC:16303, LENG7, MGC102687, MGC131894, MGC16224, PTI1, eEF1A-1, EE1A1
Protein Interaction Partner: WARS,gag,gag,gag-pol,ACTB,ARIH2,AXIN1,BRMS1,BTBD2,C11orf59,CCDC130,CCL18,CKS2,COX17,CRADD,CRCT1,CSRP2,DARS,DYNLL1,EEF1A1,EIF3F,EXOSC4,FAS,GADD45G,GUSBP1,HBXIP,HSPE1,ITSN1,KIF1B,LAMA4,LSM3,MAD2L1BP,MAGED2,MLLT3,MNAT1,MRPL42,MYOC,NEU1,ORMDL3,PABPC4,PAEP,PAFAH1B3,PAPSS1,PCDHA4,PFN2,PHYHIP,PLAUR,PLCG1,POLE2,POLR2C,PQBP1,PRKCD,PSG9,PSMD11,PTPN4,PTPRCAP,RAB27A,RFC5,RGS12,RNF10,RPA2,RPLP1,RSRC1,SARS2,SDHAF2,SERPINB9,SFN,SHBG,SMAD2,SMAD4,SSR1,STMN2,SULT1E1,TAF9,TGIF1,TMPRSS3,TP53BP2,TPT1,TRDMT1,TTR,UBQLN4,WARS,XPO5,XRN2,YWHAG,ZBTB16,ZCCHC10,ZNF24,ZNF259,ABTB2,ANKRD24,ARIH2,AXIN1,BRMS1,BTBD2,C11orf59,CCDC130,CCL18,CKS2,COX17,CRADD,CRCT1,DARS,DLEU1,DYNLL1,EIF3F,EXOSC4,FAS,HBXIP,HSPE1,ITSN1,KIF1B,LAMA4,LSM3,MAD2L1BP,MLLT3,MNAT1,MRPL42,NEU1,ORMDL3,PAEP,PAFAH1B3,PAPSS1,PCDHA4,PFN2,PHYHIP,PLAUR,PLCG1,POLE2,POLR2C,PQBP1,PSG9,PSMD11,PTPN4,PTPRCAP,RAB27A,RAF1,RFC5,RNF10,RPA2,RPLP1,RSRC1,SDHAF2,SERPINB9,SSR1,STMN2,SULT1E1,TAF9,TGIF1,TMPRSS3,TP53BP2,TRDMT1,TTR,Tmsb4x,UBC,UBQLN4,VARS,XPO5,XRN2,ZCCHC10,ZNF24,ZNF259,Zfp259
Protein Size: 462 -
Poids moléculaire
- 50 kDa
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ID gène
- 1915
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NCBI Accession
- NM_001402, NP_001393
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UniProt
- P68104
Antigène
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