ZBTB24 Antibodies

AND ZBTB24 ELISA kits, ZBTB24 Proteins

Many biological assays use antibodies to detect ZBTB24, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with ZBTB24 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop ZBTB24 antibodies...

We validate the specificity of these antibodies to ZBTB24 by testing them on tissues known to express ZBTB24 positively and negatively. Browse below to find the ZBTB24 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.

Previous: CCN4 Next: PLEKHM1

ZBTB24 Infographic by Boster Bio

All ZBTB24 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

ZBT24 (ZBTB24) (NM_014797) Human Over-expression Lysate

Human

$960
Cat # LS009841
100 µg

ZBTB24 Overview

Facts about Zinc finger and BTB domain-containing protein 24.

ZBTB24 3D structure. Source: alphafold

Zinc finger and BTB domain-containing protein 24 (ZBTB24)

May be involved in BMP2-induced transcription. .

Gene Information

Human
Gene Name:	ZBTB24
Uniprot:	O43167
Entrez:	9841

Family

Belongs to:

krueppel C2H2-type zinc-finger protein family

Alternative Names

zinc finger and BTB domain-containing protein 24; BIF1; ICF2; PATZ2; zinc finger and BTB domain containing 24; ZNF450

Molecular Weight

Mass (kDA):
78.282 kDA

Genomic Context


Human

Location:	6q21
Sequence:	6; NC_000006.12 (109462594..109483237, complement)

Tissue Specificity

Widely expressed, with highest levels in naive B-cells.

Subcellular Localizations

Nucleus.

Diseases

Immunologic Deficiency Syndromes
Developmental Delay (disorder)
Infective Disorder
Cerebral Cyst
Atherosclerosis
Gastrointestinal Infection
Congenital Anomaly Of Brain
Malignant Neoplasms
Brain Diseases

Severe Combined Immunodeficiency
Chromosome Breakage
Inflammation

Interacting Proteins

AES
BLZF1
CCNDBP1
CDA
CEP70

CEP76
HMBOX1
KLF15
KPNA3
KRT40

KRTAP10-5
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP4-2

KRTAP5-9
LDOC1
LNX1
MDFI
PHC2

POGZ
RBM10
SSX2IP
TRIM41
TSC22D4

TSGA10
ZBTB43
ZBTB8A
ZNF71

Pathways

Methylation
Dna Methylation
Transport
Intracellular Transport
Cell Development
Chromosome Breakage
Endocytosis

Secretion

PTMs

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ZBTB24

References

PMID: 21596365 by de Greef J.C., et al. Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.