Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1) Peptide
EEF1A1
Reactivity: Human
Host: Synthetic
BP, WB
Catalog No. ABIN976145
Quick Overview for Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1) Peptide (ABIN976145)
Target
eEF1A1 (EEF1A1)
(Eukaryotic Translation Elongation Factor 1 alpha 1 (EEF1A1))
Origin
Human
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Characteristics
- 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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Application Notes
- 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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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- 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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Background
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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 -
Molecular Weight
- 50 kDa
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Gene ID
- 1915
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NCBI Accession
- NM_001402, NP_001393
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UniProt
- P68104
Target
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