ZFHX4 Antibodies

AND ZFHX4 ELISA kits, ZFHX4 Proteins

Many biological assays use antibodies to detect ZFHX4, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with ZFHX4 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop ZFHX4 antibodies...

We validate the specificity of these antibodies to ZFHX4 by testing them on tissues known to express ZFHX4 positively and negatively. Browse below to find the ZFHX4 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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ZFHX4 Infographic by Boster Bio

All ZFHX4 Products

Product

Figures

Specificity

Applications

Price

Anti-Zinc finger homeobox protein 4 ZFHX4 Antibody

Human, Mouse

IHC

$380
Cat # A09122
100ul

ZFHX4 Overview

Facts about Zinc finger homeobox protein 4.

Zinc finger homeobox protein 4 (ZFHX4)

May play a role in neural and muscle differentiation (By similarity). May be involved in transcriptional regulation.

. .

Gene Information

Human
Gene Name:	ZFHX4
Uniprot:	Q86UP3
Entrez:	79776

Family

Belongs to:

krueppel C2H2-type zinc-finger protein family

Alternative Names

FLJ16514; FLJ20980; ZFH-4; ZFH4ZHF4; zinc finger homeobox 4; zinc finger homeobox protein 4; zinc finger homeodomain 4; Zinc finger homeodomain protein 4; zinc-finger homeodomain protein 4

Molecular Weight

Mass (kDA):
393.73 kDA

Genomic Context


Human

Location:	8q21.13
Sequence:	8; NC_000008.11 (76681219..76867285)

Tissue Specificity

Expressed in brain, skeletal muscle and liver. Very low expression in stomach.

Subcellular Localizations

Nucleus.

Diseases

Blepharoptosis
Sclerosis
Embryonal Carcinoma
Multiple Sclerosis
Tissue Adhesions
Congenital Camptodactyly
Muscle Hypotonia
Carcinoma
Multiple Sclerosis, Relapsing-remitting
Corneal Diseases
Micrognathism

Syndactyly
Balanced Chromosomal Translocation
Chromosomal Translocation
Congenital Ptosis
Sensorineural Hearing Loss (disorder)

Pathways

Disease Resistance
Methylation
Cell Adhesion
Axon Guidance
Localization

PTMs

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ZFHX4

References

PMID: 16946494 by Hemmi K., et al. A homeodomain-zinc finger protein, ZFHX4, is expressed in neuronal differentiation manner and suppressed in muscle differentiation manner.

PMID: 11935336 by McMullan T.W., et al. A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.