EVC2 Antibody (PACO19629)
- SKU:
- PACO19629
- Product Type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- ELISA
- WB
- IHC
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Frequently bought together:
Description
EVC2 Antibody (PACO19629)
The EVC2 Polyclonal Antibody (PAC019629) is a valuable tool for research involving EVC2, a protein associated with Ellis-van Creveld syndrome. This antibody, produced in rabbits, has high reactivity with human samples and is validated for use in various applications such as Western blot and immunohistochemistry.EVC2 is a crucial protein involved in skeletal development and is linked to the pathogenesis of Ellis-van Creveld syndrome, a rare genetic disorder characterized by skeletal abnormalities and other developmental defects. Research on EVC2 is essential for understanding the molecular mechanisms underlying this disorder and could potentially lead to the development of targeted therapies.
This antibody specifically binds to the EVC2 protein, allowing for the detection and analysis of EVC2 expression in different cell types and tissues. Its high specificity and sensitivity make it an ideal tool for studies in genetics, developmental biology, and rare diseases research. By using this antibody, researchers can further explore the role of EVC2 in normal development and disease, potentially uncovering new insights into the pathophysiology of Ellis-van Creveld syndrome.
| Antibody Name: | EVC2 Antibody (PACO19629) |
| Antibody SKU: | PACO19629 |
| Size: | 50ul |
| Host Species: | Rabbit |
| Tested Applications: | ELISA, WB, IHC |
| Recommended Dilutions: | ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:50-1:200 |
| Species Reactivity: | Human |
| Immunogen: | Synthetic peptide of human EVC2 |
| Form: | Liquid |
| Storage Buffer: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Purification Method: | Antigen affinity purification |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Conjugate: | Non-conjugated |
 | The image on the left is immunohistochemistry of paraffin-embedded Human ovarian cancer tissue using PACO19629(EVC2 Antibody) at dilution 1/40, on the right is treated with synthetic peptide. (Original magnification: x200). |
 | Gel: 6%SDS-PAGE, Lysate: 40 μg, Lane: Human placenta tissue, Primary antibody: PACO19629(EVC2 Antibody) at dilution 1/450, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 7 minutes. |
 | The image on the left is immunohistochemistry of paraffin-embedded Human colon cancer tissue using PACO19629(EVC2 Antibody) at dilution 1/40, on the right is treated with synthetic peptide. (Original magnification: x200). |
| Background: | This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. |
| Synonyms: | Ellis van Creveld syndrome 2 |
| UniProt Protein Function: | EVC2: Positive regulator of the hedgehog signaling pathway. Plays a critical role in bone formation and skeletal development. Defects in EVC2 are a cause of Ellis-van Creveld syndrome (EVC); also known as chondroectodermal dysplasia. EVC is an autosomal recessive disorder characterized by the clinical tetrad of chondrodystrophy, polydactyly, ectodermal dysplasia and cardiac anomalies. Patients manifest short-limb dwarfism, short ribs, postaxial polydactyly and dysplastic nails and teeth. Congenital heart defects, most commonly an atrioventricular septal defect, are observed in 60% of affected individuals. Defects in EVC2 are a cause of acrofacial dysostosis Weyers type (WAD); also known as Curry-Hall syndrome. Acrofacial dysostoses are a heterogeneous group of disorders combining limb defects with facial abnormalities. WAD is an autosomal dominant disorder characterized by dysplastic nails, postaxial polydactyly, acrofacial dysostosis, short limbs and short stature. The phenotype is milder than Ellis-van Creveld syndrome. 3 isoforms of the human protein are produced by alternative splicing.Protein type: Membrane protein, integralChromosomal Location of Human Ortholog: 4p16.2Cellular Component: cytoskeleton; cytoplasm; integral to membrane; nucleus; ciliumBiological Process: smoothened signaling pathwayDisease: Weyers Acrofacial Dysostosis; Ellis-van Creveld Syndrome |
| UniProt Protein Details: | |
| NCBI Summary: | This gene encodes a member of a superfamily of divalent cation-dependent phosphodiesterases. The encoded protein associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor associated factors (TRAFs), and inhibits nuclear factor-kappa-B activation. This protein has sequence and structural similarities with APE1 endonuclease, which is involved in both DNA repair and the activation of transcription factors. [provided by RefSeq, Jul 2008] |
| UniProt Code: | Q86UK5 |
| NCBI GenInfo Identifier: | 23510348 |
| NCBI Gene ID: | 51567 |
| NCBI Accession: | NP_057698 |
| UniProt Secondary Accession: | Q86UK5,Q2TBE2, Q5JYM0, Q7Z6U5, Q9NUK5, Q9NYY9, B4DKL8 B4DQ95 |
| UniProt Related Accession: | Q86UK5,O95551 |
| Molecular Weight: | 43.3 kDa (385aa) confirmed by MALDI-TOF |
| NCBI Full Name: | tyrosyl-DNA phosphodiesterase 2 |
| NCBI Synonym Full Names: | tyrosyl-DNA phosphodiesterase 2 |
| NCBI Official Symbol: | TDP2Â Â |
| NCBI Official Synonym Symbols: | EAP2; AD022; EAPII; TTRAP; hTDP2; dJ30M3.3Â Â |
| NCBI Protein Information: | tyrosyl-DNA phosphodiesterase 2 |
| UniProt Protein Name: | Limbin |
| UniProt Synonym Protein Names: | Ellis-van Creveld syndrome protein 2; EVC2 |
| Protein Family: | Limbin |
| UniProt Gene Name: | EVC2Â Â |
| UniProt Entry Name: | LBN_HUMAN |
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