Zinc finger protein 713 Antibodies

AND ZNF713 ELISA kits, Zinc finger protein 713 Proteins

Many biological assays use antibodies to detect Zinc finger protein 713, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Zinc finger protein 713 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Zinc finger protein 713 antibodies...

We validate the specificity of these antibodies to Zinc finger protein 713 by testing them on tissues known to express ZNF713 positively and negatively. Browse below to find the ZNF713 antibody that suites your experiment. We have 2 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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ZNF713 Infographic by Boster Bio

All ZNF713 Products

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Product

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Specificity

Applications

Price

Anti-ZN713 ZNF713 Antibody

Human

ELISA, WB

$380
Cat # A16565
100ul

ZNF713 (NM_182633) Human Over-expression Lysate

Human

$960
Cat # LS349075
20 µg, 100 µg

ZNF713 Overview

Facts about Zinc finger protein 713.

ZNF713 3D structure. Source: alphafold

Zinc finger protein 713 (ZNF713)

May be involved in transcriptional regulation. .

Gene Information

Human
Gene Name:	ZNF713
Uniprot:	Q8N859
Entrez:	349075

Family

Belongs to:

krueppel C2H2-type zinc-finger protein family

Alternative Names

FLJ39963; zinc finger protein 713

Molecular Weight

Mass (kDA):
50.172 kDA

Genomic Context


Human

Location:	7p11.2
Sequence:	7; NC_000007.14 (55887456..55942225)

Tissue Specificity

Expressed in fetal and adult brain.

Subcellular Localizations

Nucleus.

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ZNF713

References

PMID: 25196122 by Metsu S., et al. A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families.