DYX1C1 anticorps (AA 51-120) (Biotin)

N° du produit ABIN1700546

Détail du produit anti-DYX1C1 anticorps (Biotin)

Antigène: DYX1C1 (Dyslexia Susceptibility 1 Candidate 1 (DYX1C1))

Épitope: AA 51-120

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DYX1C1 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Réactivité croisée: Souris, Rat

Homologie: Human,Dog,Cow,Chicken,Zebrafish

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human DYX1C1

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur DYX1C1

Antigène: DYX1C1 (Dyslexia Susceptibility 1 Candidate 1 (DYX1C1))

Autre désignation: DYX1C1 (DYX1C1 Produits)

Synonymes: anticorps DYX1, anticorps DYXC1, anticorps EKN1, anticorps RD, anticorps 1700010I24Rik, anticorps Edem2, anticorps Ekn1, anticorps zgc:77853, anticorps LOC100220614, anticorps dynein axonemal assembly factor 4, anticorps dyslexia susceptibility 1 candidate 1, anticorps dynein axonemal assembly factor 4 L homeolog, anticorps DNAAF4, anticorps Dyx1c1, anticorps Dnaaf4, anticorps dnaaf4, anticorps DYX1C1, anticorps dnaaf4.L

Sujet:

Synonyms: Dyslexia susceptibility 1 candidate 1, Dyslexia susceptibility 1 candidate gene 1 protein, DYX1, DYX1C1, DYXC1, DYXC1_HUMAN, EKN1, FLJ37882, MGC70618, RD.

Background: The gene encoding DYX1C1 maps in the 15q21 region, which is disrupted by a translocation t(2,15)(q11,q21) and segregates with dyslexia. Two sequence changes in DYX1C1, including one involving the translation initiation sequence and an Elk-1 transcription factor binding site (-3G --> A) and a codon (1249G --> T), introduce a premature stop codon and truncate the protein by 4 amino acids. DYX1C1 encodes a nuclear tetratricopeptide repeat domain protein that is dynamically regulated in brain. In human brain, DYX1C1 protein localizes to a fraction of cortical neurons and white matter glial cells. It is also expressed in lung, kidney and testis.

ID gène: 161582

Pathways: Intracellular Steroid Hormone Receptor Signaling Pathway, Regulation of Intracellular Steroid Hormone Receptor Signaling