Fragile X Mental Retardation, Autosomal Homolog 2 (FXR2) Peptide
FXR2
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits FXR2
- FXR2 (Fragile X Mental Retardation, Autosomal Homolog 2 (FXR2))
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-FXR2 antibody (Catalog #: ARP40557_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.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- FXR2 (Fragile X Mental Retardation, Autosomal Homolog 2 (FXR2))
- Synonymes
- id:ibd5046 Peptide, zgc:56215 Peptide, zgc:77472 Peptide, FMR1L2 Peptide, FXR2P Peptide, Fxr2h Peptide, FMR1 autosomal homolog 2 Peptide, fragile X mental retardation, autosomal homolog 2 Peptide, FXR2 Peptide, fxr2 Peptide, Fxr2 Peptide
- Sujet
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FXR2 is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. This protein may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X mental retardation syndrome. The protein encoded by this gene is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. This encoded protein may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X mental retardation syndrome. 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: FMR1L2, FXR2P
Protein Interaction Partner: AMOTL2,AP1M1,AP2M1,ARL6IP1,C10orf62,C19orf50,CALCOCO2,CBS,CCDC33,CCDC85B,COIL,CYFIP2,DPPA2,FBP1,FMR1,FTH1,FXR1,FXR2,GKAP1,KCNRG,KCTD4,KIAA1217,KRT20,LCMT1,LDOC1,MBIP,MCRS1,MEAF6,NCK2,NECAB2,NONO,NT5C2,PAICS,PCBD1,PSME3,RABAC1,RALYL,RBBP8,RBMX,RBPMS,RPIA,RTN3,RTN4,SNAP23,SSSCA1,THAP1,TNNT1,TRAF2,TRIM29,TRIM37,TSC22D4,ZBTB8B,ZNF451,AMOTL2,AP1M1,AP2M1,ARL6IP1,C10orf62,C19orf50,CALCOCO2,CBS,CCDC33,CCDC85B,CYFIP1,DPPA2,FBP1,FMR1,FTH1,FXR1,FXR2,GKAP1,HNRNPC,KCNRG,KCTD4,KIAA1217,KRT20,LCMT1,LDOC1,MBIP,MCRS1,MEAF6,MED7,NCK2,NECAB2,NONO,NT5C2,OTUD4,PAICS,PCBD1,PSME3,RABAC1,RALYL,RBBP8,RBMX,RBPMS,RPIA,RTN3,RTN4,SNAP23,SSSCA1,THAP1,TNNT1,TRAF2,TRIM29,TRIM37,TSC22D4,ZBTB8A,ZNF451
Protein Size: 673 - Poids moléculaire
- 74 kDa
- ID gène
- 9513
- NCBI Accession
- NM_004860, NP_004851
- UniProt
- P51116
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