PKNOX1 Polyclonal antibody

PKNOX1 Polyclonal Antibody for WB, IF, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, IP, IF, IHC, ELISA

Conjugate

Unconjugated

Cat no : 10614-1-AP

Synonyms

Homeobox protein PKNOX1, Homeobox protein PREP 1, PBX/knotted 1 homeobox 1, PBX/knotted homeobox 1, PKNOX1, pkonx1c, PREP1



Tested Applications

Positive WB detected inSH-SY5Y cells, COLO 320 cells, HepG2 cells
Positive IHC detected inhuman gliomas 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

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunohistochemistry (IHC)IHC : 1:20-1:200
Immunofluorescence (IF)IF : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

10614-1-AP targets PKNOX1 in WB, IP, IF, IHC, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen PKNOX1 fusion protein Ag0939
Full Name PBX/knotted 1 homeobox 1
Calculated Molecular Weight 48 kDa
Observed Molecular Weight 50-55 kDa
GenBank Accession NumberBC007746
Gene Symbol PKNOX1
Gene ID (NCBI) 5316
RRIDAB_2164125
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen 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. 20ul sizes contain 0.1% BSA.

Protocols

Product Specific Protocols
WB protocol for PKNOX1 antibody 10614-1-APDownload protocol
IHC protocol for PKNOX1 antibody 10614-1-APDownload protocol
IF protocol for PKNOX1 antibody 10614-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB,IP

Am J Hum Genet

Gain-of-Function MN1 Truncation Variants Cause a Recognizable Syndrome with Craniofacial and Brain Abnormalities.

Authors - Noriko Miyake
mouseWB,IHC

Am J Physiol Renal Physiol

PMID: 31091119

Authors - Zhiqiang Chen