SHOX anticorps
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- Antigène Voir toutes SHOX Anticorps
- SHOX (Short Stature Homeobox (SHOX))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SHOX est non-conjugé
- Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogène
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SHOX.
- Top Product
- Discover our top product SHOX Anticorps primaire
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- Indications d'application
- SHOX antibody can be used for detection of SHOX by ELISA at 1:312500. SHOX antibody can be used for detection of SHOX by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Conseil sur la manipulation
- As with any antibody avoid repeat freeze-thaw cycles.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store SHOX antibody at -20 °C.
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- Antigène
- SHOX (Short Stature Homeobox (SHOX))
- Autre désignation
- SHOX (SHOX Produits)
- Synonymes
- anticorps si:ch211-134k13.1, anticorps zgc:123182, anticorps GCFX, anticorps PHOG, anticorps SHOXY, anticorps SS, anticorps short stature homeobox, anticorps shox, anticorps SHOX
- Sujet
- This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies.This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
- Poids moléculaire
- 32 kDa
- ID gène
- 6473
- NCBI Accession
- NP_000442
- UniProt
- O15266
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