DDX3Y anticorps (AA 70-316)

N° du produit ABIN1886628

Cet anticorps anti-DDX3Y Polyclonal Lapin (ABIN1886628) détecte spécifiquement DDX3Y dans WB et IF. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour DDX3Y anticorps (AA 70-316) (ABIN1886628)

Antigène: DDX3Y (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 3, Y-Linked (DDX3Y))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DDX3Y est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Détail du produit anti-DDX3Y anticorps

Épitope: AA 70-316

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 70 and 316 of DDX3Y

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur DDX3Y

Antigène: DDX3Y (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 3, Y-Linked (DDX3Y))

Autre désignation: DDX3Y

Sujet: DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases.They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly.Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division.This gene encodes a DEAD box protein, and it has a homolog on the X chromosome.The gene mutation causes male infertility, Sertoli cell-only syndrome or severe hypospermatogenesis, suggesting that this gene plays a key role in the spermatogenic process.Alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq]

Poids moléculaire: 73 kDa

ID gène: 8653

NCBI Accession: NP_004651, NM_004660