ZMIZ1 Antibody, FITC conjugated

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Description

Antibody Characteristics

ParameterDetails
Target ProteinZMIZ1 (Human, Mouse, Rat, and others; cross-reactivity varies by source)
EpitopeVaries by manufacturer (e.g., C-terminal, N-terminal, or internal regions)
Host SpeciesRabbit or sheep (polyclonal)
ConjugationFITC (Fluorescein Isothiocyanate)
Excitation/Emission~495 nm / ~519 nm (fluorescence imaging)
ApplicationsFlow cytometry, immunofluorescence, live-cell tracking, and IHC-Fr

Key Note: While specific FITC-conjugated ZMIZ1 antibodies are not explicitly listed in the provided sources, standard conjugation practices suggest suppliers like R&D Systems, antibodies-online, and VWR offer FITC-labeled variants tailored for fluorescent detection .

Detection of ZMIZ1 Localization and Activity

  • Immunofluorescence (IF): FITC-conjugated ZMIZ1 antibodies enable visualization of nuclear or cytoplasmic ZMIZ1 localization in fixed or live cells. For example, ZMIZ1 is reported to localize to nuclei in human ovary sections and lymphatic endothelial cells (LECs) .

  • Flow Cytometry: Quantifies ZMIZ1 expression levels in cell populations. This is critical for studying ZMIZ1’s role in diseases like vitiligo, where its overexpression promotes melanocyte proliferation and migration .

  • Live-Cell Imaging: FITC’s photostability allows real-time tracking of ZMIZ1 dynamics during processes like lymphatic valve formation .

Mechanistic Studies in Disease Models

Disease/ModelZMIZ1’s RoleMethodology
VitiligoPromotes melanocyte proliferation/migration; inhibits apoptosis .MTT assay, Transwell migration, flow cytometry
Tongue Squamous Cell Carcinoma (TSCC)Enhances invasion/metastasis via Notch1 signaling .RNAi knockdown, CCK-8 assay, lung metastasis models
Lymphatic Vascular DefectsRegulates Prox1 expression and LEC valve density .ATAC-seq, RNA-Seq, lymphatic-specific knockout mice

ZMIZ1 in Melanocyte Biology

  • Vitiligo Pathogenesis: Overexpression of ZMIZ1 in melanocyte cell lines (e.g., PIG1, PIG3V) increases proliferation, reduces apoptosis, and enhances migration. FITC-conjugated antibodies could track ZMIZ1’s subcellular distribution during these processes .

  • Cytoskeletal Remodeling: ZMIZ1 knockdown alters actin cytoskeleton structure, impairing cell migration. Fluorescent imaging with FITC-labeled antibodies could visualize cytoskeletal dynamics .

ZMIZ1 in Cancer

  • TSCC Progression: ZMIZ1 knockdown reduces Notch1/Jagged1 signaling and metastasis-related factors (MMP7, MKP-1). FITC-conjugated antibodies may aid in assessing ZMIZ1’s interaction with Notch1 in real-time .

  • Lymphatic Endothelial Cells (LECs): ZMIZ1 regulates Prox1 expression by modifying chromatin accessibility at its regulatory regions. FITC-labeled antibodies could map ZMIZ1’s recruitment to Prox1 enhancers during lymphangiogenesis .

ZMIZ1 in Vascular Development

  • Yolk Sac Vasculature: Global ZMIZ1 knockout mice exhibit embryonic lethality due to defective yolk sac vascularization. FITC-conjugated antibodies may trace ZMIZ1’s role in endothelial cell survival or migration .

Comparison of ZMIZ1 Antibodies

Catalog NumberEpitopeHostConjugationApplications
AF8107

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Typically, we can ship your orders within 1-3 business days of receipt. Delivery times may vary depending on the purchase method and location. Please consult your local distributor for specific delivery timeframes.
Synonyms
hZIMP10 antibody; KIAA1224 antibody; MIZ antibody; PIAS like protein hZimp10 antibody; PIAS like protein on chromosome 10 antibody; PIAS like protein Zimp10 antibody; PIAS-like protein Zimp10 antibody; RAI 17 antibody; Retinoic acid induced 17 antibody; Retinoic acid induced protein 17 antibody; Retinoic acid-induced protein 17 antibody; TRAFIP10 antibody; Zimp10 antibody; Zinc finger containing Miz1 PIAS like protein on chromosome 10 antibody; Zinc finger MIZ domain-containing protein 1 antibody; Zinc finger MIZ-type containing 1 antibody; Zmiz1 antibody; ZMIZ1_HUMAN antibody
Target Names
ZMIZ1
Uniprot No.

Target Background

Function
ZMIZ1, also known as Zimp10, is a transcriptional coactivator that plays a crucial role in regulating various cellular processes. It enhances the ligand-dependent transcriptional activity of the androgen receptor (AR) and promotes AR sumoylation, which is essential for its activity. ZMIZ1 also functions as a transcriptional coactivator in the TGF-beta signaling pathway by increasing the activity of the SMAD3/SMAD4 transcriptional complex. Moreover, ZMIZ1 is involved in the transcriptional activation of a subset of NOTCH1 target genes, including MYC, and plays a role in thymocyte and T cell development. It also contributes to the regulation of postmitotic positioning of pyramidal neurons during cerebral cortex development.
Gene References Into Functions
  1. A genome-wide association study and subsequent replication study identified a significant (P<5 x 10(-8)) association between rs76518691 in the ZMIZ1 gene and rs7523831 near NGF, and primary dysmenorrhea in Chinese women. PMID: 28447608
  2. Research has identified a molecular phenotype of Multiple Sclerosis (MS) characterized by the expression of the MS risk gene ZMIZ1 in blood, along with other genes, particularly transcription factors. Notably, ZMIZ1 expression is influenced by and interacts with environmental risk factors such as Epstein-Barr virus (EBV) and Vitamin D. PMID: 28063629
  3. The variants rs1250569 (ZMIZ1) and rs10114470 (TL1A) have been identified as novel loci associated with susceptibility to Inflammatory Bowel Disease in Han-Chinese patients. PMID: 28456797
  4. This case provides valuable insights into the potential function and effects of MIZ-type containing and proline-rich 12 in the central nervous system, as it represents the first constitutional balanced translocation disrupting and fusing these two elements. PMID: 26163108
  5. Research at the ZMIZ1 locus has revealed that perturbation of ZMIZ1 expression in human islets and beta-cells impacts exocytosis and insulin secretion, highlighting a novel role for ZMIZ1 in maintaining glucose homeostasis. PMID: 26624892
  6. Targeting the interaction between NOTCH1 and ZMIZ1 could potentially be a strategy for combating leukemic growth. PMID: 26522984
  7. The expression of SENP8, SAE1, PIAS1, PIAS2, and ZMIZ1 is dysregulated in the majority of papillary thyroid carcinoma (PTC) tissues, suggesting a potential contribution to the PTC phenotype. PMID: 26403403
  8. ZMIZ1 has been identified as a susceptibility gene for vitiligo in the Chinese population. PMID: 24667117
  9. ZMIZ1 is overexpressed in a significant proportion of human breast, ovarian, and colon cancers, as well as squamous cell carcinomas, suggesting a broader role in epithelial cancers. PMID: 23426136
  10. ZMIZ1 and activated NOTCH1 are coexpressed in a subset of human T-cell acute lymphoblastic leukemia (T-ALL) patients and cell lines. PMID: 23161489
  11. Evidence suggests a physiological role for endogenous Zimp10 in regulating Smad3/4-mediated transcription. PMID: 16777850
  12. RAI17 was found to be upregulated in WT-Add1 compared to MUT-Add1 overexpressing cells, potentially representing a key molecule/axis for the functional Add1-induced effect. PMID: 17512505
  13. Expression of exogenous hZimp10 enhances the transcriptional activity of p53, while knockdown of endogenous hZimp10 reduces the transcriptional activity of p53. PMID: 17584785
  14. Research provides evidence supporting a crucial role for Zimp10 in vasculogenesis. PMID: 17967885
  15. Fusion of ZMIZ1 to ABL1 is associated with a B-cell acute lymphoblastic leukemia with a t(9;10)(q34;q22.3) translocation. PMID: 18007576

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Database Links

HGNC: 16493

OMIM: 607159

KEGG: hsa:57178

STRING: 9606.ENSP00000334474

UniGene: Hs.193118

Subcellular Location
Nucleus, nucleoplasm. Cytoplasm. Nucleus.
Tissue Specificity
Expressed most abundantly in ovary and, at lower levels, in prostate, spleen and testis. Weak expression, if any, in thymus, small intestine, colon and peripheral blood leukocytes.

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