ECT2 Antibody, Biotin conjugated

Shipped with Ice Packs
In Stock

Description

Introduction to ECT2 Antibody, Biotin Conjugated

The Epithelial Cell Transforming Sequence 2 (ECT2) Antibody, Biotin Conjugated is a specialized immunological reagent designed to detect and study the ECT2 protein, a guanine nucleotide exchange factor (GEF) critical in regulating Rho GTPases and cellular processes such as cytokinesis and ribosomal biogenesis . Biotin conjugation enhances the antibody’s utility in assays requiring signal amplification, leveraging the high-affinity interaction between biotin and streptavidin/avidin systems .

2.1. Epitope Specificity and Antibody Design

ECT2 antibodies target specific amino acid regions of the protein:

AntibodyEpitope (AA)HostConjugateReactivityApplications
ABIN7165314 283–453RabbitBiotinHumanELISA
ABIN5531087 597–625RabbitUnconjugatedHumanWB, IHC (p)
26557-1-AP Full-lengthRabbitUnconjugatedHumanWB, IF/ICC, FC (Intra)
ABIN129688 785–795 (pThr790)RabbitUnconjugatedHumanWB, ELISA, IP
Abbexa (Biotin) N/ARabbitBiotinHumanWB, IHC, IF/ICC

Key Features:

  • Polyclonal Rabbit Origin: Ensures broad epitope recognition .

  • Biotin Conjugation: Enables detection via streptavidin-HRP, streptavidin-Alexa Fluor, or streptavidin-coated beads .

  • Phospho-Specific Variants: Detect phosphorylated ECT2 (e.g., pThr790), critical for studying mitotic regulation .

3.1. Assay Optimization

Biotin-conjugated ECT2 antibodies amplify signals in:

MethodPurposeExample Protocol
ELISAQuantify ECT2 levels in lysates or serumBiotin-ECT2 + streptavidin-HRP
Western BlotAnalyze ECT2 isoforms or phosphorylation statusBiotin-ECT2 + streptavidin-IR dye
ImmunoprecipitationIsolate ECT2-protein complexes (e.g., UBF1 in ribosomal DNA transcription) Biotin-ECT2 + streptavidin-agarose beads
ImmunofluorescenceVisualize ECT2 localization in mitotic cells or nucleoliBiotin-ECT2 + streptavidin-Alexa 488

Dilution Guidelines:

ApplicationRecommended Dilution
WB1:500–1:3000
IHC1:10–1:50
IF/ICC1:200–1:800
Flow Cytometry0.25 µg/10⁶ cells

4.1. Role in Cytokinesis and Oncogenesis

ECT2 regulates Rho GTPases (e.g., RhoA, Rac1, Cdc42) during cell division. Biotin-conjugated antibodies have elucidated:

  • Mitotic Localization: ECT2 spreads throughout the cytoplasm during prometaphase and condenses in the midbody during cytokinesis .

  • Phosphorylation-Dependent Activity: Phosphorylation at Thr790 enhances ECT2’s GEF activity, critical for mitotic progression .

4.2. ECT2-UBF1 Interaction in Ribosomal Biogenesis

In non-small-cell lung cancer (NSCLC), ECT2 binds the transcription factor UBF1 on ribosomal DNA (rDNA) promoters:

  • BRCT Domain Dependency: The ECT2 BRCT domain mediates interaction with phosphorylated UBF1 (Ser412) .

  • PKCι-Mediated Phosphorylation: Protein kinase Cι (PKCι) phosphorylates UBF1, enabling ECT2 recruitment and rRNA synthesis .

4.3. Therapeutic Implications

  • Cancer Targeting: Overexpression of ECT2 in tumors correlates with aggressive growth. Biotin-conjugated antibodies enable precise detection for diagnostic or therapeutic monitoring .

  • Universal CAR T Cells: Biotin-streptavidin systems enhance tumor targeting, as demonstrated in HER2+ breast and pancreatic cancers .

Table 1: ECT2 Antibody Comparisons

SupplierCatalog #EpitopeConjugateKey Applications
Antibodies-onlineABIN7165314 AA 283–453BiotinELISA
Antibodies-onlineABIN5531087 AA 597–625UnconjugatedWB, IHC (p)
Proteintech26557-1-AP Full-lengthUnconjugatedWB, IF/ICC, FC (Intra)
AbbexaN/A N/ABiotinWB, IHC, IF/ICC

Table 2: Molecular and Functional Characteristics

ParameterDetails
Molecular Weight100–104 kDa
Gene ID1894 (Human)
UniProtQ9H8V3
PathwaysNeurotrophin signaling, cell-cell junction organization, ribosomal biogenesis

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 time may vary depending on the shipping method and destination. Please consult your local distributors for specific delivery details.
Synonyms
ECT2Protein ECT2 antibody; Epithelial cell-transforming sequence 2 oncogene antibody
Target Names
ECT2
Uniprot No.

Target Background

Function
ECT2 (Epithelial Cell Transforming Sequence 2) is a guanine nucleotide exchange factor (GEF) that facilitates the exchange of GDP for GTP. It promotes guanine nucleotide exchange on Rho family members of small GTPases, including RHOA, RHOC, RAC1, and CDC42. This activity is essential for signal transduction pathways involved in regulating cytokinesis, the process of cell division. ECT2 is a component of the centralspindlin complex, which serves as a microtubule-dependent and Rho-mediated signaling pathway crucial for myosin contractile ring formation during cytokinesis. ECT2 regulates the translocation of RHOA from the central spindle to the equatorial region, playing a role in controlling mitotic spindle assembly and regulating CDC42 activation in metaphase for spindle fiber attachment to kinetochores before chromosome congression. ECT2 is involved in regulating epithelial cell polarity and participates in the formation of epithelial tight junctions within the PARD3-PARD6-protein kinase PRKCQ polarity complex. It also contributes to the regulation of neurite outgrowth and inhibits phenobarbital (PB)-induced NR1I3 nuclear translocation. ECT2 stimulates the activity of RAC1 through its association with the oncogenic PARD6A-PRKCI complex in cancer cells, driving tumor cell proliferation and invasion. Furthermore, ECT2 stimulates genotoxic stress-induced RHOB activity in breast cancer cells, leading to their death.
Gene References Into Functions
  1. High ECT2 expression has been correlated with tumor metastasis and poor overall survival in osteosarcoma patients. PMID: 28794404
  2. The expression of ECT2 is linked to the survival of patients with breast cancer, and its high expression is significantly associated with unfavorable survival rates. PMID: 29051317
  3. Research has identified p53 as a novel upstream signaling molecule of ECT2 in Gastric cancer cells. PMID: 28654632
  4. High PDC2 expression has been associated with pancreatic adenocarcinoma. PMID: 26993610
  5. While ECT2 association with the plasma membrane is essential for cytokinesis, evidence suggests that ECT2 recruitment to the spindle midzone may not fully account for equatorial furrowing and might act redundantly with other unidentified signals. PMID: 27926870
  6. Among 518 genes co-expressed with ECT2 in LUAD and 386 genes co-expressed with ECT2 in LUSC, there were only 98 genes in the overlapping cluster. PMID: 29088286
  7. E6AP suppresses breast cancer metastasis by regulating actin cytoskeleton remodeling through the control of ECT2 and Rho GTPase activity. PMID: 27231202
  8. Ect2 regulates rRNA synthesis through a PKCiota-Ect2-Rac1-NPM signaling axis that is required for lung tumorigenesis. PMID: 28110998
  9. Data suggests that the expression of epithelial cell transforming sequence 2 oncogene (ECT2) can serve as an alternative measurement that can compensate for the inadequacy of the current carcinoembryonic antigen (CEA) test in the diagnosis and monitoring of colorectal cancer patients. PMID: 28362321
  10. Research demonstrates that the cytokinetic proteins epithelial cell transforming 2 and Aurora kinase B (AurkB) are localized to stress granules in human astrocytoma cells. PMID: 27106762
  11. Kaplan-Meier analysis revealed that lower levels of Ect2 mRNA predicted higher overall survivals and biochemical recurrence (BCR)-free survivals in all patients or non-metastatic patients. PMID: 28012134
  12. Findings suggest that ECT2 plays a significant role during gastric cancer progression. PMID: 26497353
  13. Colorectal cancer patients with high expression levels of ECT2 had shorter overall survival. PMID: 26211594
  14. ECT2 can interact with RACGAP1 to catalyze the GTP exchange involved in Rho signaling, further regulating tumor initiation and metastasis. PMID: 25617497
  15. Up-regulation of ECT2 might contribute to the progression of gastric carcinogenesis and may be a valuable prognostic indicator in gastric cancer. PMID: 25674238
  16. Poly(ADP-ribosyl)ation is recognized by ECT2. PMID: 25486481
  17. Central spindle assembly and two Plk1-dependent phosphorylations are required to establish efficient binding of the Ect2 BRCT in early cytokinesis. PMID: 25486482
  18. ECT2 expression is positively correlated with WHO pathologic grading and unfavorable survival, suggesting that ECT2 may be a potential therapeutic target in human gliomas. PMID: 25237947
  19. Structural analysis of the triple-BRCT domain of ECT2 provides insights into the binding characteristics to CYK-4. PMID: 25068414
  20. Deregulation of miR-223 and its target gene ECT2 may be associated with the aggressive tumor progression of human osteosarcoma. PMID: 24784921
  21. Abnormality of the ECT2 gene occurs at a relatively early stage of lung adenocarcinogenesis and could be a new biomarker for prognostication of patients with lung adenocarcinoma. PMID: 24484057
  22. Both Pbl and ECT2 repress Wg/Wnt target gene expression in cultured Drosophila and human cells. PMID: 24198276
  23. Data suggests that ECT2 may play an oncogenic role in the pancreatic ductal adenocarcinoma (PDAC) neoplastic process. PMID: 23851435
  24. miR-223 functions as a tumor suppressor in osteosarcoma, and the miR-223/Ect2/p21 signaling pathway plays a crucial role in regulating osteosarcoma cell cycle progression and proliferation. PMID: 23601845
  25. ECT2 is essential for tight junction function and maintaining cell polarity. Dysfunction of this gene may lead to renal tubulointerstitial injury, progressing to glomerular sclerosis. PMID: 22552385
  26. RASAL2 has been identified as an ECT2-interacting protein that regulates RHO activity in astrocytoma cells. PMID: 22683310
  27. Research indicates that Ect2 becomes active in prophase, where it is exported from the nucleus to the cytoplasm, activating RhoA to induce the formation of a mechanically stiff and rounded metaphase cortex. PMID: 22898780
  28. Data supports an analogous function for the anillin-Ect2 complex in human cells. One hypothesis is that this complex functionally replaces the Drosophila anillin-RacGAP50C complex. PMID: 22514687
  29. Ect2 is identified as a cell cycle-regulated protein, suggesting that its ubiquitination-dependent degradation may play a significant role in RhoA regulation during mitosis. PMID: 21886810
  30. The targeting of Ect2 to the equatorial membrane is a key step in delivering the cytokinetic signal to the cortex. PMID: 22172673
  31. A mechanism involving the nuclear GEFs Ect2 and Net1 for activating RhoB after genotoxic stress, facilitating cell death following treatment with DNA damaging agents has been proposed. PMID: 21373644
  32. Ect2 has been suggested as a potential regulator of matrix-contact-side localization of invadopodia-related proteins. PMID: 21474972
  33. A model has been proposed where PKCiota-mediated phosphorylation regulates Ect2 binding to the oncogenic PKCiota-Par6 complex, thereby activating Rac1 activity and driving transformed growth and invasion. PMID: 21189248
  34. Results suggest that ECT2 is an indicator of cellular proliferation in OSCCs and that ECT2 might be a potential therapeutic target for the development of new treatments for OSCCs. PMID: 21124766
  35. XRCC1, CLB6, and BRCT domains of ECT2 play a critical role in regulating cytokinesis. PMID: 14587037
  36. ECT2 regulates the polarity complex Par6/Par3/PKCzeta and potentially plays a role in epithelial cell polarity. PMID: 15254234
  37. BRCT domains negatively regulate Ect2 GEF activity in interphase cells and are also required for the proper function of Ect2 during cytokinesis. PMID: 15545273
  38. Ect2 regulates the activation and function of Cdc42 in mitosis. PMID: 15642749
  39. Central spindle localization of ECT2 assists division plane positioning, and the CYK-4 subunit of centralspindlin acts upstream of RhoA to promote furrow assembly. PMID: 16103226
  40. Cdk1 inactivation is sufficient to activate a signaling pathway leading to cytokinesis, which emanates from mitotic spindles and is regulated by ECT2, MgcRacGAP, and RhoA. PMID: 16118207
  41. MgcRacGAP controls the initiation of cytokinesis by regulating ECT2, which in turn induces the assembly of the contractile ring and triggers the ingression of the cleavage furrow. PMID: 16129829
  42. Evidence suggests a conformational change of ECT2 upon phosphorylation at T341, implying that ECT2 activity might be regulated by the phosphorylation status of T341. PMID: 16170345
  43. ECT2 is regulated by Plk1 and CDK1, and phosphorylation of ECT2 leads to accumulation of RHOA. PMID: 16247472
  44. Research shows that RhoA accumulates at the equatorial cortex before furrow initiation and continues to concentrate at the cleavage furrow during cytokinesis. Centralspindlin and ECT2 are required for this localization and furrowing. PMID: 16352658
  45. ECT2 knockdown triggers cell cycle arrest in G1. PMID: 16778203
  46. In mitotic cells, Ect2 localizes to the central spindle and the cell cortex. PMID: 16803869
  47. Aberrant ECT2 expression, observed in various human tumors, could be the direct result of RB/E2F pathway deficiency, contributing to cell division in cancers. PMID: 16862181
  48. Late mitotic Plk1 activity promotes recruitment of Ect2 to the central spindle, triggering the initiation of cytokinesis and contributing to cleavage plane specification in human cells. PMID: 17488623
  49. This gene was silenced. PMID: 17688947
  50. Results suggest that equatorial Ect2 locally suppresses lamellipodia formation via RhoA activation, which indirectly contributes to restricting lamellipodia formation to polar regions during cytokinesis B. PMID: 17942602

Show More

Hide All

Database Links

HGNC: 3155

OMIM: 600586

KEGG: hsa:1894

STRING: 9606.ENSP00000232458

UniGene: Hs.518299

Subcellular Location
Nucleus. Cytoplasm. Cytoplasm, cytoskeleton, spindle. Cleavage furrow. Midbody. Cell junction. Cell junction, tight junction. Note=Sequestered within the nucleus during interphase. Dispersed throughout the cytoplasm upon breakdown of the nuclear envelope during mitosis. Colocalizes with the centralspindlin complex to the mitotic spindles during anaphase/metaphase, the cleavage furrow during telophase and at the midbody at the end of cytokinesis. Colocalized with RhoA at the midbody. Its subcellular localization to tight junction is increased by calcium. Localized predominantly in the cytoplasm of numerous carcinoma cells.
Tissue Specificity
Expressed in lung epithelial cells (at protein level). Expressed in squamous cell carcinoma, primary non-small cell lung cancer tumors and lung adenocarcinoma.

Quick Inquiry

Personal Email Detected
Please use an institutional or corporate email address for inquiries. Personal email accounts ( such as Gmail, Yahoo, and Outlook) are not accepted. *
© Copyright 2025 TheBiotek. All Rights Reserved.