DLX3 anticorps (AA 40-120)
Aperçu rapide pour DLX3 anticorps (AA 40-120) (ABIN7214576)
Antigène
Voir toutes DLX3 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 40-120
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Fonction
- Dlx-3 Polyclonal Antibody
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Specificité
- Dlx-3 Polyclonal Antibody detects endogenous levels of Dlx-3 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogène
- Synthesized peptide derived from the Internal region of human Dlx-3 at AA range: 40-120
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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Commentaires
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- DLX3 (Distal-Less Homeobox 3 (DLX3))
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Autre désignation
- Dlx-3
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Sujet
- Rabbit Anti-Dlx-3 Polyclonal Antibody,DLX3, Homeobox protein DLX-3,Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in DLX3 have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.,Homeobox protein DLX-3
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Poids moléculaire
- observerd band 45kDa
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ID gène
- 1747
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UniProt
- O60479
Antigène
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