AFF2 anticorps (N-Term)
-
- Antigène Voir toutes AFF2 Anticorps
- AFF2 (AF4/FMR2 Family, Member 2 (AFF2))
-
Épitope
- N-Term
-
Reactivité
- Humain, Souris, Boeuf (Vache)
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp AFF2 est non-conjugé
-
Application
- Western Blotting (WB)
- Séquence
- MDLFDFFRDW DLEQQCHYEQ DRSALKKREW ERRNQEVQQE DDLFSSGFDL
- Réactivité croisée (Details)
- Species reactivity (expected):Mouse, Rat, Horse, Rabbit, Guinea PigSpecies reactivity (tested):Human
- Purification
- Purified using peptide immunoaffinity column
- Immunogène
- Synthetic peptide directed towards the N terminal of human AFF2
- Top Product
- Discover our top product AFF2 Anticorps primaire
-
-
- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
-
- Reconstitution
- Add 50 μL of distilled water to a final concentration of 1 mg/mL.
- Conseil sur la manipulation
- Avoid repeated freezing and thawing.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
-
- Antigène
- AFF2 (AF4/FMR2 Family, Member 2 (AFF2))
- Autre désignation
- AFF2 / FMR2 (AFF2 Produits)
- Synonymes
- anticorps FMR2, anticorps FMR2P, anticorps FRAXE, anticorps MRX2, anticorps OX19, anticorps Fmr2, anticorps Ox19, anticorps Oxh, anticorps AF4/FMR2 family member 2, anticorps AF4/FMR2 family, member 2, anticorps AFF2, anticorps Aff2
- Sujet
- AFF2 is a RNA-binding protein and might be involved in alternative splicing regulation through an interaction with G-quartet RNA structure. Defects in AFF2 are the cause of mental retardation X-linked associated with fragile site FRAXE (MRFRAXE). A form of mild to moderate mental retardation associated with learning difficulties, communication deficits, attention problems, hyperactivity, and autistic behavior. It is associated with a fragile site on chromosome Xq28.Synonyms: AF4/FMR2 family member 2, Fragile X E mental retardation syndrome protein, Fragile X mental retardation 2 protein, Protein Ox19
- ID gène
- 2334
- NCBI Accession
- NP_002016
-