Zinc finger protein 142 Antibodies

AND ZNF142 ELISA kits, Zinc finger protein 142 Proteins

Many biological assays use antibodies to detect Zinc finger protein 142, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Zinc finger protein 142 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Zinc finger protein 142 antibodies...

We validate the specificity of these antibodies to Zinc finger protein 142 by testing them on tissues known to express ZNF142 positively and negatively. Browse below to find the ZNF142 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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ZNF142 Infographic by Boster Bio

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ZNF142 (NM_001105537) Human Over-expression Lysate

Human

$960
Cat # LS007701
20 µg, 100 µg

ZNF142 Overview

Facts about Zinc finger protein 142.

ZNF142 3D structure. Source: alphafold

Zinc finger protein 142 (ZNF142)

May be involved in transcriptional regulation. .

Gene Information

Human
Gene Name:	ZNF142
Uniprot:	P52746
Entrez:	7701

Family

Belongs to:

krueppel C2H2-type zinc-finger protein family

Alternative Names

Zinc finger protein 142

Molecular Weight

Mass (kDA):
187.88 kDA

Genomic Context


Human

Location:	2q35
Sequence:	2; NC_000002.12 (218633329..218659623, complement)

Subcellular Localizations

Nucleus.

PTMs

Isopeptide bond

Phosphoprotein

Ubl conjugation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ZNF142

References

PMID: 7557990 by Tommerup N., et al. Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders.

PMID: 31036918 by Khan K., et al. Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.