FOXP2 anticorps (C-Term)
Aperçu rapide pour FOXP2 anticorps (C-Term) (ABIN263146)
Antigène
Voir toutes FOXP2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Classe de qualité
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Épitope
- C-Term
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Fonction
- FOXP2 (C terminus)
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Séquence
- REIEEEPLSE DLE
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Specificité
- This antibody is expected to recognise all three reported isoforms (NP_055306.1, NP_683696.2, NP_683697.1).
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Réactivité croisée
- Boeuf (Vache), Chien, Humain, Souris, Porc, Rat
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Purification
- Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
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Immunogène
- Peptide with sequence C-REIEEEPLSEDLE, from the C Terminus of the protein sequence according to NP_055306.1, NP_683696.2, NP_683697.1.
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Isotype
- IgG
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Indications d'application
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Western Blot: Approx 80-90 kDa band observed in Human Brain (Cerebellum) lysates (calculated MW of 82.6 kDa according to NP_683696.2). This molecular weight is routinely observed by other sources. Recommended concentration: 0.5-2 μg/mL. Primary incubation
Peptide ELISA: antibody detection limit dilution 1:128000.
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Supplied at 0.5 mg/mL in Tris saline, 0.02 % sodium azide, pH 7.3 with 0.5 % bovine serum albumin.
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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
- Minimize freezing and thawing.
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Stock
- -20 °C
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Stockage commentaire
- Aliquot and store at -20°C, with minimal freeze/thawing. A working aliquot may be refrigerated at 4°C for a few weeks and still remain viable.
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: "Cerebellar nuclei excitatory neurons regulate developmental scaling of presynaptic Purkinje cell number and organ growth." dans: eLife, Vol. 8, (2020) (PubMed).
: "Wfs1- deficient rats develop primary symptoms of Wolfram syndrome: insulin-dependent diabetes, optic nerve atrophy and medullary degeneration." dans: Scientific reports, Vol. 7, Issue 1, pp. 10220, (2019) (PubMed).
: "Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms." dans: eLife, Vol. 6, (2017) (PubMed).
: "Clustered fine compartmentalization of the mouse embryonic cerebellar cortex and its rearrangement into the postnatal striped configuration." dans: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 32, Issue 45, pp. 15688-703, (2012) (PubMed).
: "FoxP2 expression in the cerebellum and inferior olive: development of the transverse stripe-shaped expression pattern in the mouse cerebellar cortex." dans: The Journal of comparative neurology, Vol. 520, Issue 3, pp. 656-77, (2011) (PubMed).
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: "Cerebellar nuclei excitatory neurons regulate developmental scaling of presynaptic Purkinje cell number and organ growth." dans: eLife, Vol. 8, (2020) (PubMed).
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- FOXP2 (Forkhead Box P2 (FOXP2))
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Autre désignation
- FOXP2
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Sujet
- FOXP2, forkhead box P2, SPCH1, CAGH44, TNRC10, CAG repeat protein 44, speech and language disorder 1, trinucleotide repeat containing 10, forkhead/winged-helix transcription factor, DKFZp686H1726, OTTHUMP00000196932
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ID gène
- 93986
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NCBI Accession
- NP_055306, NP_683696, NP_683697
Antigène
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