Zinc finger protein 674 Antibodies

AND ZNF674 ELISA kits, Zinc finger protein 674 Proteins

Many biological assays use antibodies to detect Zinc finger protein 674, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Zinc finger protein 674 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Zinc finger protein 674 antibodies...

We validate the specificity of these antibodies to Zinc finger protein 674 by testing them on tissues known to express ZNF674 positively and negatively. Browse below to find the ZNF674 antibody that suites your experiment. We have 0 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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ZNF674 Infographic by Boster Bio

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ZNF674 Overview

Facts about Zinc finger protein 674.

ZNF674 3D structure. Source: alphafold

Zinc finger protein 674 (ZNF674)

May be involved in transcriptional regulation. .

Gene Information

Human
Gene Name:	ZNF674
Uniprot:	Q2M3X9
Entrez:	641339

Family

Belongs to:

krueppel C2H2-type zinc-finger protein family

Alternative Names

MRX92; zinc finger protein 674

Molecular Weight

Mass (kDA):
67.199 kDA

Genomic Context


Human

Location:	Xp11.3
Sequence:	X; NC_000023.11 (46497725..46545466, complement)

Tissue Specificity

Expressed in testis.

Subcellular Localizations

Nucleus.

Diseases

Retinal Dystrophies
Dystrophy
Sclerosis
Learning Disabilities
Genetic Diseases, X-linked
Developmental Delay (disorder)
Fraxa Syndrome
Developmental Disabilities
Autistic Disorder

Dwarfism
Tuberous Sclerosis
Visual Impairment

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ZNF674

References

PMID: 16385466 by Lugtenberg D., et al. ZNF674: a new Kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

PMID: 23871722 by Piton A., et al. XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.