ZBTB20 Antibody

Code CSB-PA867198ESR1HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human adrenal gland tissue using CSB-PA867198ESR1HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) ZBTB20 Polyclonal antibody
Uniprot No.
Target Names
ZBTB20
Alternative Names
Dendritic derived BTB/POZ zinc finger protein antibody; Dendritic-derived BTB/POZ zinc finger protein antibody; DKFZp566F123 antibody; DPZF antibody; HOF antibody; ODA 8S antibody; OTTHUMP00000215066 antibody; OTTHUMP00000215067 antibody; OTTHUMP00000215069 antibody; OTTHUMP00000215071 antibody; ZBT20_HUMAN antibody; Zbtb20 antibody; zinc finger 288 antibody; zinc finger and BTB domain containing 20 antibody; Zinc finger and BTB domain-containing protein 20 antibody; Zinc finger protein 288 antibody; ZNF288 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Zinc finger and BTB domain-containing protein 20 protein (100-400AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
May be a transcription factor that may be involved in hematopoiesis, oncogenesis, and immune responses. Plays a role in postnatal myogenesis, may be involved in the regulation of satellite cells self-renewal.
Gene References into Functions
  1. ZBTB20 knockdown inhibited glioblastoma cell proliferation, migration, and invasion. PMID: 30099442
  2. High ZBTB20 expression is associated with hepatocellular carcinoma. PMID: 26893361
  3. We report a boy with intellectual disability carrying two de novo missense mutations in the last exon of ZBTB20 (Ser616Phe and Gly741Arg; both previously unreported). One of them, Ser616Phe, affects an amino acid located in one of the C2H2 zing-fingers involved in DNA-binding and close to other missense mutations already described. Reverse phenotyping showed that this patient presents with classic features of Primrose syn PMID: 27061120
  4. ZBTB20 rs9841504 polymorphism is a protective factor for gastric cancer rather than esophageal cancer. PMID: 27646774
  5. 3q13.31 microdeletion-based dosage imbalance of ZBTB20 linked to a range of neurodevelopmental, cognitive and psychiatric disorders, likely mediated by dysregulation of multiple ZBTB20 target genes. PMID: 25062845
  6. Major depressive disorder is associated with significant hypermethylation within the coding region of ZBTB20. PMID: 24694013
  7. important role for ZBTB20 in controlling NSCLC development PMID: 25311537
  8. Missense mutations in ZBTB20 underlie Primrose syndrome. PMID: 25017102
  9. This study disclosed Zbtb20-mediated transcriptional repressor mechanism may be involved in development of the human archicortex. PMID: 23283686
  10. Polymorphism in ZBTB20 gene is associated with gastric cancer. PMID: 23861218
  11. We identified new susceptibility loci for non-cardia gastric cancer at 3q13.31: rs9841504 in ZBTB20 PMID: 22037551
  12. ZBTB20 mRNA & protein expression were elevated significantly in HCC tissues compared with the paired non-tumor tissues & normal liver. HCC recurrence or metastasis increased & disease-free survival decreased with high ZBTB20 expression. PMID: 21702992
  13. Misexpression of Zbtb20 in transgenic mice converts the normal cytoarchitectonic organization of the subiculum, postsubiculum, and granular retrosplenial cortex to a CA1-like stratum pyramidale. PMID: 19955470

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Involvement in disease
Primrose syndrome (PRIMS)
Subcellular Location
Nucleus.
Tissue Specificity
Expressed in spleen, lymph node, thymus, peripheral blood leukocytes, and fetal liver.
Database Links

HGNC: 13503

OMIM: 259050

KEGG: hsa:26137

STRING: 9606.ENSP00000419153

UniGene: Hs.202577

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