ESR1 (Ab-104) Antibody

Shipped with Ice Packs
In Stock

Description

Basic Characteristics

The antibody possesses the following fundamental properties:

PropertySpecification
Host SpeciesRabbit
Species ReactivityHuman, Mouse
Antibody TypePolyclonal
ClonalityPolyclonal
IsotypeIgG
ConjugationNon-conjugated
TargetESR1 (Estrogen Receptor alpha)
Target AliasesER, ESR, ESR1, ESTR, ESTRA
UniProt IDP03372

The antibody specifically recognizes the estrogen receptor alpha protein, which functions as a nuclear hormone receptor involved in the regulation of eukaryotic gene expression and affects cellular proliferation and differentiation in target tissues .

Physical Properties and Formulation

The antibody is supplied in a stabilized liquid formulation with specific buffer components:

PropertySpecification
Concentration1.0 mg/mL
Buffer CompositionPhosphate buffered saline (without Mg²⁺ and Ca²⁺), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol
FormLiquid
Size100 μL
Purification MethodAffinity chromatography using epitope-specific peptide

This formulation ensures stability during storage and minimizes background interference during experimental applications .

Manufacturing Process and Quality Control

The production of ESR1 (Ab-104) Antibody follows standardized immunological procedures to ensure consistent quality and specificity.

Immunogen and Production

The antibody is generated through a systematic immunization process:

  1. Synthetic peptide corresponding to amino acids 102-106 (S-V-S-P-S) of human estrogen receptor alpha is conjugated to KLH (Keyhole Limpet Hemocyanin) carrier protein

  2. Rabbits are immunized with this conjugated peptide

  3. Serum is collected and processed for antibody isolation

  4. The antibodies undergo purification via affinity chromatography using the epitope-specific peptide

This approach yields high-specificity antibodies against the target epitope while minimizing non-specific binding to other cellular proteins.

Validated Applications and Protocols

ESR1 (Ab-104) Antibody has been validated for multiple research applications, each with specific recommended protocols and dilutions.

Application Range

The antibody performs effectively in the following experimental contexts:

ApplicationRecommended Dilution
Western Blot (WB)1:500-1:1000
Immunohistochemistry (IHC)1:50-1:200
ELISA1:2000-1:10000

These applications allow researchers to detect and analyze ESR1 expression across various experimental systems .

Application Examples

Experimental validation of the antibody has been documented in specific research contexts:

  1. Western Blot Analysis: The antibody effectively detects ESR1 protein in extracts from MCF-7 breast cancer cell lines, demonstrating specificity for the target protein .

  2. Immunohistochemistry: The antibody has been successfully employed for immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue. Specificity has been confirmed through blocking peptide experiments, which showed elimination of staining when the antibody was pre-incubated with the immunizing peptide .

These validated applications highlight the antibody's utility in cancer research, particularly in studies involving estrogen receptor-positive breast cancer models.

ESR1 Biological Context and Research Significance

Understanding the biological context of ESR1 provides valuable perspective on the research significance of ESR1 (Ab-104) Antibody.

ESR1 Biological Function

Estrogen receptor alpha (ESR1) is a member of the nuclear receptor superfamily, functioning primarily as a ligand-activated transcription factor. Upon binding estrogen, ESR1:

  1. Undergoes dimerization and intranuclear translocation

  2. Binds to estrogen response elements (EREs) on DNA

  3. Regulates transcription of downstream genes

  4. Can also activate rapid non-genomic signaling pathways

ESR1 is expressed in various tissues including mammary gland, uterus, skeleton, and cardiovascular system, playing crucial roles in maintaining physiological functions of these tissues .

ESR1 in Disease Context

ESR1 has significant implications in multiple disease states, particularly:

  1. Breast Cancer: ESR1 is a key driver in many breast cancers, with approximately 70% of breast cancers classified as ER-positive

  2. Endocrine Resistance: Mutations in ESR1 (especially around amino acids 536-538) are associated with acquired resistance to endocrine therapy in metastatic breast cancer, occurring in up to 40% of ER+, HER2- metastatic cases

  3. Subtype Switching: Recent research indicates that ESR1 mutations can induce basal marker expression in luminal breast cancer cells, suggesting a role in subtype plasticity

These contexts highlight the importance of specific antibodies like ESR1 (Ab-104) in studying ESR1 protein modification, localization, and function.

Post-Translational Modifications

ESR1 undergoes multiple post-translational modifications that regulate its activity, including phosphorylation at serine residues 104, 106, 118, and 167. The region targeted by ESR1 (Ab-104) Antibody (amino acids 102-106) contains serine 104, which is a known phosphorylation site that influences AF-1 dependent transcriptional activity .

Research Applications in ESR1 Mutant Breast Cancer

Recent studies examining ESR1 mutations reveal compelling research applications for ESR1 (Ab-104) Antibody.

ESR1 Mutations and Phenotypic Changes

Current research has identified that ESR1 mutant tumors display distinct phenotypic characteristics:

  1. Significant enrichment of basal subtype markers, particularly basal cytokeratins (BCKs)

  2. Chromatin reprogramming centered around progesterone receptor-orchestrated insulated neighborhoods

  3. Enriched immune pathways, with increased expression of immune mediators such as S100A8 and S100A9

  4. Altered paracrine signaling in the tumor microenvironment

The antibody targeting the region around amino acids 102-106 can help detect wild-type ESR1 expression levels in comparison to mutant forms, potentially contributing to research on resistance mechanisms.

Diagnostic and Therapeutic Implications

The application of ESR1 antibodies in research extends to potential diagnostic and therapeutic approaches:

  1. Monitoring ESR1 expression levels in response to endocrine therapy

  2. Studying the changes in ESR1 localization and function in mutant contexts

  3. Evaluating the efficacy of novel therapeutic strategies targeting ESR1-dependent pathways

These applications underscore the importance of well-characterized antibodies in translational research bridging basic science and clinical applications.

Comparative Analysis with Other ESR1 Antibodies

When selecting an appropriate antibody for ESR1 research, it's important to consider how ESR1 (Ab-104) Antibody compares to other available options.

Target Epitope Considerations

Different ESR1 antibodies target distinct epitopes that may be differently accessible depending on:

  1. Protein conformation

  2. Presence of post-translational modifications

  3. Protein-protein interactions

  4. Mutation status

ESR1 (Ab-104) Antibody specifically targets the region around amino acids 102-106, which is distinct from the ligand-binding domain (where many clinically relevant mutations occur). This makes it potentially useful for detecting total ESR1 levels regardless of mutation status in the ligand-binding domain .

Product Specs

Form
Supplied at 1.0mg/mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Lead Time
Generally, we can ship the products within 1-3 business days after receiving your orders. Delivery time may vary depending on the purchase method or location. For specific delivery time, please consult your local distributors.
Synonyms
7*/654 isoform antibody; 7*/819 2 isoform antibody; 7*/822 isoform antibody; 8*/901 isoform antibody; 8*/941 isoform antibody; DKFZp686N23123 antibody; ER alpha antibody; ER antibody; ER-alpha antibody; Era antibody; ESR antibody; ESR1 antibody; ESR1_HUMAN antibody; ESRA antibody; Estradiol receptor antibody; Estrogen nuclear receptor alpha antibody; Estrogen receptor 1 antibody; Estrogen receptor alpha 3*,4,5,6,7*/822 isoform antibody; Estrogen receptor alpha antibody; Estrogen receptor alpha delta 3*,4,5,6,7*,8*/941 isoform antibody; Estrogen receptor alpha delta 3*,4,5,6,7*/819 2 isoform antibody; Estrogen receptor alpha delta 4 +49 isoform antibody; Estrogen receptor alpha delta 4*,5,6,7*/654 isoform antibody; Estrogen receptor alpha delta 4*,5,6,7,8*/901 isoform antibody; Estrogen receptor alpha E1 E2 1 2 antibody; Estrogen receptor alpha E1 N2 E2 1 2 antibody; Estrogen receptor antibody; ESTRR antibody; NR3A1 antibody; Nuclear receptor subfamily 3 group A member 1 antibody
Target Names
Uniprot No.

Target Background

Function
The estrogen receptor alpha (ERα) is a nuclear hormone receptor that plays a crucial role in regulating eukaryotic gene expression. It is involved in various cellular processes including proliferation and differentiation in target tissues. ERα mediates its function through ligand-dependent nuclear transactivation, involving direct homodimer binding to an estrogen response element (ERE) sequence or association with other DNA-binding transcription factors such as AP-1/c-Jun, c-Fos, ATF-2, Sp1, and Sp3, to mediate ERE-independent signaling. Ligand binding triggers a conformational change in ERα, enabling subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Additionally, ERα exhibits mutual transrepression with NF-kappa-B in a cell-type-specific manner. It decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter, displacing RELA/p65 and associated coregulators from the promoter. ERα is recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters, potentially displacing CREBBP. It co-localizes with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Furthermore, ERα can synergistically activate transcription with NF-kappa-B by recruiting adjacent response elements, a process involving CREBBP. ERα can also activate the transcriptional activity of TFF1. Moreover, it mediates membrane-initiated estrogen signaling involving various kinase cascades. ERα is essential for MTA1-mediated transcriptional regulation of BRCA1 and BCAS3 and is involved in activating NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are believed to modulate transcriptional activity through competitive ligand or DNA binding and/or heterodimerization with the full-length receptor. Notably, ERα binds to ERE and inhibits isoform 1.
Gene References Into Functions
  1. Estrogen-induced miR-191 has been identified as a direct upstream regulator of DAB2 in ER-positive breast cancer cells. PMID: 29247596
  2. This research provides comprehensive genome-wide insights that contribute to a deeper understanding of ER1's biological roles in breast cancer. PMID: 30301189
  3. The study revealed a correlation between rs2046210 and rs3803662, and the risk of developing breast cancer in Vietnamese women. The A allele is identified as the risk allele for both rs2046210 (OR [95% CI] = 1.43 [1.14 - 1.78], P = 0.0015) and rs3803662 (OR [95% CI] = 1.45 [1.16 - 1.83], P = 0.001). The findings indicate that two polymorphisms, rs2046210 in ESR1 and rs3803662 in TNRC9, are associated with breast cancer risk in the Vietnamese population. PMID: 30078824
  4. The study demonstrated that estrogen receptor alpha can enhance odonto/osteogenic differentiation of stem cells from apical papilla via ERK and JNK MAPK pathways. PMID: 30069950
  5. No association was found between polymorphisms in genes encoding estrogen receptors (ESR1 and ESR2) and excreted BPA levels in orthodontic patients after bracket bonding. PMID: 29961922
  6. Analysis of genome-wide ER binding sites revealed mutant ER unique recruitment mediating the allele-specific transcriptional program. PMID: 29438694
  7. The study identified RNF8 as a co-activator of ERalpha that enhances ERalpha stability via a post-transcriptional pathway. This finding provides a new perspective on the mechanisms by which RNF8 promotes cell growth in ERalpha-positive breast cancer. PMID: 28216286
  8. Reduced expression of ERbeta1 in female ERalpha-negative papillary thyroid carcinoma patients is associated with greater disease progression. PMID: 29655286
  9. ERα and ERβ exhibit a heterogeneous distribution in deep infiltrating endometriosis. PMID: 29383962
  10. The ER-alpha36/EGFR signaling loop promotes the growth of hepatocellular carcinoma cells. PMID: 29481815
  11. The study investigated the presence and localization of estrogen receptors (ERs), progesterone receptors (PRs), and androgen receptors (ARs) in both healthy and varicose vein wall cells and their relationship with gender. PMID: 30250632
  12. Estrogen receptor-alpha expression was observed only in women and showed a positive correlation with the amount of fungi in oral paracoccidioidomycosis. Progesterone receptor was present in both genders but exhibited no correlation with estrogen receptor-alpha or fungi counting. PMID: 29796757
  13. ERalpha upregulates vinculin expression in breast cancer cells, while loss of vinculin promotes amoeboid features of cancer cells. PMID: 28266545
  14. Polymorphisms in the ERα gene do not predict in vitro fertilization outcome. PMID: 29916276
  15. High ESR1 expression is associated with metastasis in breast cancer. PMID: 29187405
  16. The G/G XbaI genotype of the ESR1 gene is associated with breast cancer risk. PMID: 29893332
  17. miR-221 may impair the protective effect of estrogen in degenerated cartilaginous endplate cells by targeting estrogen receptor alpha. PMID: 29529124
  18. The study found that NAT1 and ESR1 expression were elevated in primary breast tumor samples compared to normal breast tissue samples, and in ER+ primary breast tumors compared to ER- tumors. The study suggests that NAT1 and ESR1 expression may share overlapping regulation. PMID: 29901116
  19. All patients without mutations detected by molecular barcode next-generation sequencing (MB-NGS) were confirmed to have no mutations by ddPCR. The study concluded that MB-NGS successfully detected ESR1 mutations in cfDNA with a higher sensitivity (0.1%) than conventional NGS and demonstrated clinical utility comparable to ddPCR. PMID: 28905136
  20. The study identified an association between specific genotypes at three ESR1 polymorphisms (rs2234693, rs6902771, rs7774230) and one ESR2 polymorphism (rs3020449) and the presence of metabolic syndrome in postmenopausal women. PMID: 30049354
  21. The study observed a higher frequency of ESR1 and PIK3CA mutations in plasma compared to serum in 33 MBC patients, suggesting that serum samples may not be the preferred source of cfDNA. PMID: 29689710
  22. The findings suggest that miR-125a-3p may function as a novel tumor suppressor in ER(+) breast cancer by targeting CDK3, potentially offering a therapeutic approach for TamR breast cancer therapy. PMID: 28939591
  23. A significant finding of the study revealed that 20% of patients with breast cancer bone marrow (BM) exhibited receptor discrepancy between the primary tumor and subsequent BM, with loss of hormone receptors (ER and/or PR) expression and gain of HER2 overexpression being the most common changes. PMID: 28975433
  24. The research highlights a pivotal role for IGF-IR in regulating ERalpha-positive breast cancer cell aggressiveness and the regulation of expression levels of several extracellular matrix molecules. PMID: 28079144
  25. The study explored the associations between PvuII (T>C) and XbaI (A>G) polymorphisms of the estrogen receptor alpha (ESR1) gene with type 2 diabetes mellitus (T2DM) or metabolic syndrome (MetS). PMID: 29883973
  26. The ERalpha gene appears to play a key role in stress urinary incontinence during the premenopausal period. PMID: 29769420
  27. The study reported the first discovery of naturally occurring ESR1 (Y537C) and ESR1 (Y537S) mutations in MCF7 and SUM44 ESR1-positive cell lines following acquired resistance to long-term estrogen deprivation (LTED) and subsequent resistance to fulvestrant (ICIR). These mutations accumulated over time, impacting ESR1 binding to the genome and altering the ESR1 interactome. PMID: 29192207
  28. Concomitant high expression of ERalpha36, GRP78, and GRP94 is associated with aggressive papillary thyroid cancer behavior and can serve as a predictor for extrathyroid extension, lymph node metastasis, and distant metastasis. PMID: 29368272
  29. Estrogen receptor-1 is a key regulator of HIV-1 latency and imparts gender-specific restrictions on the latent reservoir. PMID: 30061382
  30. Down-regulation of ESR1 gene expression was enhanced by the development of breast cancer. PMID: 29543921
  31. The study aimed to assess whether fibrosis markers, estrogen receptor (ER)alpha, and the stromal derived factor (SDF)1/CXC chemokine receptor type 4 (CXCR4) axis are abnormally expressed in the endometrium of patients with intrauterine adhesions. PMID: 29568895
  32. The frequency of alleles and genotypes of polymorphisms FSHR(-29G/A) and ESRI (XbaI A/G) in women with normal to poor response did not show significant correlation. PMID: 29526845
  33. Each estrogen receptor alpha and estrogen receptor beta gene polymorphism may have a differential impact on postmenopausal osteoporosis risk and bone mineral density across various ethnicities. PMID: 29458346
  34. The results suggest that the minor allele A of the ESR1 gene is associated with the development of arterial hypertension in men. PMID: 29658078
  35. The study found that tamoxifen treatment induced a decrease in PRMT2 and an increase in ER-alpha36 as well as ER-alpha36-mediated non-genomic effect in the MDA-MB-231 breast cancer cell line. PMID: 29620287
  36. ESR1 mutations are not associated with clinical resistance to fulvestrant in breast cancer patients. PMID: 27174596
  37. Overexpression of COPS5, through its isopeptidase activity, leads to ubiquitination and proteasome-mediated degradation of NCoR, a key corepressor for ERalpha and tamoxifen-mediated suppression of ERalpha target genes. PMID: 27375289
  38. ESR alpha PvuII and XbaI polymorphisms are not associated with systemic lupus erythematosus. However, the combination of the TC/AA and CC/GG genotypes was associated with SLE susceptibility. PMID: 29356461
  39. Estrogen receptor (ER) and progesterone receptor (PR) expression in endometrial carcinoma (EC) were significantly higher than those in the paracarcinoma tissue and control. PMID: 29081408
  40. ESR1 promoter methylation was identified as an independent risk factor and exhibited a high predictive value for 28-day mortality from acute-on-chronic hepatitis B liver failure. PMID: 29082740
  41. By analyzing different estrogen receptor-alpha(ER-a)-positive and ER-a-negative breast cancer cell lines, the study defined the role of CCN5 in the leptin-mediated regulation of growth and invasive capacity. PMID: 29370782
  42. This study identified ESR1 as a direct target of miR-301a-3p. PMID: 29763890
  43. Authors report for the first time the presence of ESR1 methylation in plasma ctDNA of patients with HGSC. The agreement between ESR1 methylation in primary tumors and paired ctDNA was statistically significant. PMID: 29807696
  44. This study reports the development of a novel class of ERa AF2 inhibitors, which have the potential to effectively inhibit ERa activity by a unique mechanism and to circumvent the issue of mutation-driven resistance in breast cancer. PMID: 29462880
  45. The P2X7R rs3751143 and ER-alpha PvuII two-locus interaction confers a significantly high susceptibility to osteoporosis in Chinese postmenopausal women. PMID: 28884379
  46. Alcohol consumption may have differential effects on concordant and discordant receptor subtypes of breast cancer. PMID: 29353824
  47. ERalpha and ERbeta mRNA expression was significantly higher (p < 0.05) in tumor tissues compared to their paired normal mucosa and correlated inversely with survival outcome. PMID: 29390981
  48. High ESR1 expression is associated with Papillary Thyroid Carcinoma. PMID: 28124274
  49. Oral administration of RAD140 substantially inhibited the growth of AR/ER(+) breast cancer patient-derived xenografts (PDX). Activation of the AR and suppression of the ER pathway, including the ESR1 gene, were observed with RAD140 treatment. PMID: 28974548
  50. Polymorphism in the ERalpha gene is associated with an increased risk for advanced Pelvic Organ Prolapse. However, polymorphism in the LAMC1 gene does not appear to be associated with such risk. PMID: 29241914

Show More

Hide All

Database Links

HGNC: 3467

OMIM: 133430

KEGG: hsa:2099

STRING: 9606.ENSP00000206249

UniGene: Hs.208124

Involvement In Disease
Estrogen resistance (ESTRR)
Protein Families
Nuclear hormone receptor family, NR3 subfamily
Subcellular Location
[Isoform 1]: Nucleus. Cytoplasm. Cell membrane; Peripheral membrane protein; Cytoplasmic side.; Nucleus. Golgi apparatus. Cell membrane. Note=Colocalizes with ZDHHC7 and ZDHHC21 in the Golgi apparatus where most probably palmitoylation occurs. Associated with the plasma membrane when palmitoylated.
Tissue Specificity
Widely expressed. Not expressed in the pituitary gland.; [Isoform 3]: Widely expressed, however not expressed in the pituitary gland.

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.