Zinc finger protein 512B Antibodies

AND ZNF512B ELISA kits, Zinc finger protein 512B Proteins

Many biological assays use antibodies to detect Zinc finger protein 512B, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Zinc finger protein 512B in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Zinc finger protein 512B antibodies...

We validate the specificity of these antibodies to Zinc finger protein 512B by testing them on tissues known to express ZNF512B positively and negatively. Browse below to find the ZNF512B 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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ZNF512B Infographic by Boster Bio

All ZNF512B Products

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Specificity

Applications

Price

ZNF512B (NM_020713) Human Over-expression Lysate

Human

$960
Cat # LS057473
100 µg

ZNF512B Overview

Facts about Zinc finger protein 512B.

ZNF512B 3D structure. Source: alphafold

Zinc finger protein 512B (ZNF512B)

May be involved in transcriptional regulation. .

Gene Information

Human
Gene Name:	ZNF512B
Uniprot:	Q96KM6
Entrez:	57473

Family

Belongs to:

krueppel C2H2-type zinc-finger protein family

Alternative Names

GM632; KIAA1196; MGC149845; MGC149846; zinc finger protein 512B

Molecular Weight

Mass (kDA):
97.264 kDA

Genomic Context


Human

Location:	20q13.33
Sequence:	20; NC_000020.11 (63956703..63969930, complement)

Subcellular Localizations

Nucleus.

Diseases

Sclerosis
Primary Lateral Sclerosis
Amyotrophic Lateral Sclerosis
Neurodegenerative Disorders
Cholangiocarcinoma
Spinal And Bulbar Muscular Atrophy, X-linked 1
Spastic Paraplegia, Hereditary
Muscular Atrophy
Atrophy
Hypokinesia

Motor Neuron Disease
Paraplegia
Malignant Neoplasms
Spastic Paraplegia
Spinal Muscular Atrophy

Interacting Proteins

FHL3
SIAH1
TRAF1

Pathways

Pathogenesis
Cell Proliferation

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ZNF512B

References

PMID: 11780052 by Deloukas P., et al. The DNA sequence and comparative analysis of human chromosome 20.

PMID: 10574462 by Nagase T., et al. Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.