ALX Homeobox 3 (ALX3) Cell ELISA Kit

513.5€ (96 tests)
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935106861
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name
ALX Homeobox 3 (ALX3) Cell ELISA Kit
category
ELISA Kits
provider
Abbexa
reference
abx595688
tested applications
ELISA
Description
ALX3 Cell ELISA Kit is a cell-based ELISA Kit. Cells to be assayed should be seeded onto a clear flat bottom 96 well plate, using poly-L-lysine for non-adherent cells. Cells should be grown to 75-90% confluence and treated prior to carrying out the ELISA.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | ELISA Kits |
Immunogen Target | ALX Homeobox 3 (ALX3) |
Reactivity | Human, Mouse, Rat |
Detection Method | Colorimetric |
Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
Size 1 | 96 tests |
Tested Applications | ELISA |
Availability | Shipped within 1-2 weeks. The validity for this kit is at least 6 months |
Storage | Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual. |
Dry Ice | No |
UniProt ID | O95076 |
Gene ID | 257 |
OMIM | 136760 |
Alias | FND,FND1 |
Background | Elisa kits for ALX3 |
Status | RUO |
Note | Validity: 6 months. This product is for research use only. The range and sensitivity is subject to change. Please contact us for the latest product information. For accurate results, sample concentrations must be diluted to mid-range of the kit. If you require a specific range, please contact us in advance or write your request in your order comments. Please note that our ELISA and CLIA kits are optimised for detection of native samples, rather than recombinant proteins. We are unable to guarantee detection of recombinant proteins, as they may have different sequences or tertiary structures to the native protein. |
Descripción
ALX3 is a transcription factor belonging to the homeobox gene family, which regulates developmental processes, including craniofacial development, limb formation, and neural crest cell differentiation. ALX3 is expressed in facial mesenchymal tissues during embryogenesis, where it controls genes necessary for midline and upper facial development. Mutations or dysregulation of ALX3 are linked to frontonasal dysplasia, characterized by cleft lip/palate, hypertelorism, and nasal malformations. ALX3 has been shown to interact with other transcription factors and signaling pathways to regulate the proliferation and migration of mesenchymal cells. Emerging studies suggest ALX3 may act as a tumor suppressor in certain cancers, as its expression has been shown to inhibit cell proliferation and epithelial-mesenchymal transition (EMT). Its role in regulating gene expression during development and disease highlights ALX3 as a potential target for understanding congenital malformations and tumorigenesis.
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