UBQLN2 Polyclonal antibody

UBQLN2 Polyclonal Antibody for IF, IHC, WB,ELISA

Host / Isotype

Rabbit / IgG


human, rat and More (1)





Cat no : 23449-1-AP


CHAP1, CHAP1/DSK2, Dsk2, DSK2 homolog, hPLIC 2, HRIHFB2157, LIC 2, N4BP4, PLIC 2, PLIC2, RIHFB2157, ubiquilin 2, Ubiquilin-2, UBQLN2

Tested Applications

Positive WB detected inrat brain tissue, HEK-293 cells, HepG2 cells
Positive IHC detected inhuman testis tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF detected inHepG2 cells, A431 cells

Recommended dilution

Western Blot (WB)WB : 1:500-1:1000
Immunohistochemistry (IHC)IHC : 1:50-1:500
Immunofluorescence (IF)IF : 1:20-1:200
Sample-dependent, check data in validation data gallery

Product Information

The immunogen of 23449-1-AP is UBQLN2 Fusion Protein expressed in E. coli.

Tested Reactivity human, rat
Cited Reactivitymouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen UBQLN2 fusion protein Ag20149
Full Name ubiquilin 2
Calculated molecular weight 624 aa, 66 kDa
Observed molecular weight 66-70 kDa
GenBank accession numberBC069237
Gene symbol UBQLN2
Gene ID (NCBI) 29978
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.


Product Specific Protocols
WB protocol for UBQLN2 antibody 23449-1-APDownload protocol
IHC protocol for UBQLN2 antibody 23449-1-APDownload protocol
IF protocol for UBQLN2 antibody 23449-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols



Hum Mol Genet

Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.

Authors - Aline Dubos

Brain Pathol

Serpin neuropathology in the P497S UBQLN2 mouse model of ALS/FTD.

Authors - Nicole R Higgins

J Neurochem

Pathogenic mutation of UBQLN2 impairs its interaction with UBXD8 and disrupts endoplasmic reticulum-associated protein degradation.

Authors - Yuxing Xia