MYT1L anticorps (AA 195-825)

N° du produit ABIN7871706

L’anticorps anti-MYT1L Polyclonal Lapin est utilisé pour la détection de MYT1L dans des échantillons de Humain. Il a été validé pour WB, ELISA, IF et FACS.

Aperçu rapide pour MYT1L anticorps (AA 195-825) (ABIN7871706)

Antigène: MYT1L (Myelin Transcription Factor 1-Like (MYT1L))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYT1L est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Détail du produit anti-MYT1L anticorps

Épitope: AA 195-825

Fonction: MYT1L Antibody / Myelin transcription factor 1-like protein

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (D195-K825) was used as the immunogen for the MYT1L antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the MYT1L antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the MYT1L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur MYT1L

Antigène: MYT1L (Myelin Transcription Factor 1-Like (MYT1L))

Autre désignation: MYT1L

Sujet: Myelin transcription factor 1 like is a protein that in humans is encoded by the MYT1L gene. This gene encodes a member of the zinc finger superfamily of transcription factors whose expression, thus far, has been found only in neuronal tissues. The encoded protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in this gene have been associated with an autosomal dominant form of cognitive disability and with autism spectrum disorder. Alternative splicing results in multiple variants.

UniProt: Q9UL68