DAXX Polyclonal antibody

DAXX Polyclonal Antibody for IF, WB,ELISA

Host / Isotype

Rabbit / IgG


human, mouse





Cat no : 20489-1-AP


BING2, DAP6, DAXX, EAP1, ETS1 associated protein 1, hDaxx

Tested Applications

Positive WB detected inY79 cells, HeLa cells
Positive IF detected inA431 cells

Recommended dilution

Western Blot (WB)WB : 1:500-1:3000
Immunofluorescence (IF)IF : 1:20-1:200
Sample-dependent, check data in validation data gallery

Published Applications

WBSee 1 publications below

Product Information

The immunogen of 20489-1-AP is DAXX Fusion Protein expressed in E. coli.

Tested Reactivity human, mouse
Cited Reactivity mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen DAXX fusion protein Ag14519
Full Name death-domain associated protein
Calculated molecular weight 740 aa, 81 kDa
Observed molecular weight 120 kDa, 70 kDa
GenBank accession numberBC109074
Gene symbol DAXX
Gene ID (NCBI) 1616
Conjugate Unconjugated
Form Liquid
Purification Method Antigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

Death associated protein 6 (DAXX) is a ubiquitous protein implicated in various cellular processes such as apoptosis, tumorigenesis, developmentand transcription. It has been shown to translocate from the nucleus to the cytoplasm under conditions of stress and to activate the Jun N-terminal kinase (JNK) pathway. Somatic mutations of death associated protein (DAXX) have been found in ALT cancers, including pancreatic neuroendocrine (panNET) cancers and glioblastoma multiforme (GBM) cancers.


Product Specific Protocols
WB protocol for DAXX antibody 20489-1-APDownload protocol
IF protocol for DAXX antibody 20489-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols



J Biol Chem

The histone chaperone Spt6 is required for activation-induced cytidine deaminase target determination through H3K4me3 regulation.

Authors - Nasim A Begum