CA9 Antibodies
Background
Carbonic anhydrase IX encoded by the CA9 gene is a zinc metalloenzyme anchored to the cell membrane and mainly exists on the surface of certain tumor cells. This enzyme participates in regulating the pH balance of the cellular microenvironment by catalyzing the hydration of carbon dioxide to generate carbonic acid and protons, supporting the survival and invasion of tumor cells under hypoxic conditions. Due to the presence of hypoxia-responsive elements in its promoter region, CA9 is significantly highly expressed in various solid tumors such as renal cell carcinoma. This characteristic makes it an important tumor biomarker and target for targeted therapy research. CA9 was first identified in 1994. Its unique structure and function not only deepened people's understanding of the tumor metabolic adaptation mechanism, but also provided a key molecular basis for the development of new cancer diagnostic tools and inhibitor drugs.
Structure of CA9
CA9 is a transmembrane protein with a molecular weight of approximately 54-58 kDa. Its size may vary slightly depending on the degree of glycosylation modification. This protein is composed of 459 amino acids and contains an extracellular catalytic domain, a transmembrane region and an intracellular short tail. The active center of CA9 has a zinc ion binding site, which is the key to its catalytic reversible hydration reaction of carbon dioxide. Its extracellular region contains conserved carbonic anhydrase characteristic sequences and stabilizes the spatial conformation through disulfide bonds. The expression of CA9 is significantly upregulated mainly in solid tumors, especially showing high specificity in clear cell renal cell carcinoma. Its protein structure and function make it an important research object for tumor-targeted therapy.
Fig. 1 Linkage disequilibrium (LD) and haplotype block structure of the CA9 gene.1
Key structural properties of CA9:
- Extracellular carbonic anhydrase domain
- Transmembrane anchor regions maintain protein membrane localization
- Intracellular short tails are involved in signal transduction
Functions of CA9
The main function of the CA9 gene is to regulate cell pH and promote tumor adaptation to hypoxic environments. In addition, it is also involved in various pathological processes such as cell proliferation, migration and metastasis.
| Function | Description |
| Acid-base regulation | Catalyze the hydration of CO₂ to form carbonic acid and protons, acidify the tumor microenvironment, and promote tumor invasion and metastasis. |
| Adaptation to hypoxia | Under hypoxic conditions, it is highly expressed induced by HIF-1α, helping tumor cells survive in the hypoxic microenvironment. |
| Cell adhesion and migration | Through the structure of extracellular domain involved in signaling between cells, affect tumor cell adhesion and athletic ability. |
| Cancer progression | Its overexpression is associated with the poor prognosis of various cancers, promoting tumor growth, angiogenesis and treatment resistance. |
| Diagnosis and targeted therapy | As a biomarker for various solid tumors such as renal cell carcinoma, it is used in molecular imaging and targeted drug development. |
The activity of CA9 depends on zinc ion cofactors. Its enzymatic kinetic characteristics are characterized by high catalytic efficiency and adaptability to acidic environments, playing a key role in tumor metabolic reprogramming.
Applications of CA9 and CA9 Antibody in Literature
1. Yin, Lingdi, et al. "CA9-related acidic microenvironment mediates CD8+ T cell related immunosuppression in pancreatic cancer." Frontiers in Oncology 11 (2022): 832315. https://doi.org/10.3389/fonc.2021.832315
This study integrated multi-omics data and found that pancreatic cancer cells highly express the CA9 gene. It inhibits CD8⁺T cell infiltration by mediating an acidic microenvironment, promotes immune escape, and affects patient prognosis, providing a new direction for immunotargeted therapy.
2. Guan, Chenyu, et al. "CA9 transcriptional expression determines prognosis and tumour grade in tongue squamous cell carcinoma patients." Journal of cellular and molecular medicine 24.10 (2020): 5832-5841. https://doi.org/10.1111/jcmm.15252
This study, based on TCGA data analysis, found that CA9 is highly expressed in tongue squamous cell carcinoma and is associated with prognosis and tumor grade. CA9 promotes tumor progression by regulating cell differentiation, apoptosis, hypoxia and signaling pathways such as PI3K/AKT/mTOR, but has no significant association with immune infiltration.
3. Xu, Jiatong, et al. "CA9 silencing promotes mitochondrial biogenesis, increases putrescine toxicity and decreases cell motility to suppress ccRCC progression." International journal of molecular sciences 21.16 (2020): 5939. https://doi.org/10.3390/ijms21165939
This study confirmed that CA9 is highly expressed in clear cell renal cell carcinoma. Knockdown of CA9 can inhibit proliferation by up-regulating ARG2 and accumulating putrescine, and reduce migration by down-regulating extracellular matrix interaction and amino acid transport, indicating that CA9 is a potential therapeutic target.
4. Hudson, Amanda L., et al. "CA9, CYFIP2 and LGALS3BP—A Novel Biomarker Panel to Aid Prognostication in Glioma." Cancers 16.5 (2024): 1069. https://doi.org/10.3390/cancers16051069
This study aims to discover prognostic biomarkers for glioma progression. Verification revealed that CA9, CYFIP2 and LGALS3BP are associated with progression, and a three-protein combination panel was constructed, which can effectively distinguish the long and short survival periods of patients and has significant clinical potential.
5. Zhao, Kunming, et al. "LncRNA ZNF674-AS1 drives cell growth and inhibits cisplatin-induced pyroptosis via up-regulating CA9 in neuroblastoma." Cell Death & Disease 15.1 (2024): 5. https://doi.org/10.1038/s41419-023-06394-8
This study reveals that lncRNA ZNF674-AS1 stabilizes CA9 mRNA by binding to IGF2BP3, thereby upregulating CA9 expression, promoting the proliferation of neuroblastoma and cisplatin resistance. Targeting this axis can provide a new treatment strategy.
Creative Biolabs: CA9 Antibodies for Research
Creative Biolabs specializes in the production of high-quality CA9 antibodies for research and industrial applications. Our portfolio includes monoclonal antibodies tailored for ELISA, Flow Cytometry, Western blot, immunohistochemistry, and other diagnostic methodologies.
- Custom CA9 Antibody Development: Tailor-made solutions to meet specific research requirements.
- Bulk Production: Large-scale antibody manufacturing for industry partners.
- Technical Support: Expert consultation for protocol optimization and troubleshooting.
- Aliquoting Services: Conveniently sized aliquots for long-term storage and consistent experimental outcomes.
For more details on our CA9 antibodies, custom preparations, or technical support, contact us at email.
Reference
- Chien, Ming-Hsien, et al. "Impacts of CA9 gene polymorphisms and environmental factors on oral-cancer susceptibility and clinicopathologic characteristics in Taiwan." PloS one 7.12 (2012): e51051. https://doi.org/10.1371/journal.pone.0051051
Anti-CA9 antibodies
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- AActivation
- AGAgonist
- APApoptosis
- BBlocking
- BABioassay
- BIBioimaging
- CImmunohistochemistry-Frozen Sections
- CIChromatin Immunoprecipitation
- CTCytotoxicity
- CSCostimulation
- DDepletion
- DBDot Blot
- EELISA
- ECELISA(Cap)
- EDELISA(Det)
- ESELISpot
- EMElectron Microscopy
- FFlow Cytometry
- FNFunction Assay
- GSGel Supershift
- IInhibition
- IAEnzyme Immunoassay
- ICImmunocytochemistry
- IDImmunodiffusion
- IEImmunoelectrophoresis
- IFImmunofluorescence
- IGImmunochromatography
- IHImmunohistochemistry
- IMImmunomicroscopy
- IOImmunoassay
- IPImmunoprecipitation
- ISIntracellular Staining for Flow Cytometry
- LALuminex Assay
- LFLateral Flow Immunoassay
- MMicroarray
- MCMass Cytometry/CyTOF
- MDMeDIP
- MSElectrophoretic Mobility Shift Assay
- NNeutralization
- PImmunohistologyp-Paraffin Sections
- PAPeptide Array
- PEPeptide ELISA
- PLProximity Ligation Assay
- RRadioimmunoassay
- SStimulation
- SESandwich ELISA
- SHIn situ hybridization
- TCTissue Culture
- WBWestern Blot




