Homeobox D13 anticorps (N-Term)
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- Antigène Voir toutes Homeobox D13 (HOXD13) Anticorps
- Homeobox D13 (HOXD13)
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Épitope
- N-Term
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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 Homeobox D13 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- ASGFAYPGTS ERTGSSSSSS SSAVVAARPE APPAKECPAP TPAAAAAAPP
- Attributs du produit
- This is a rabbit polyclonal antibody against HXD13. It was validated on Western Blot.
- Purification
- Affinity purified
- Immunogène
- The immunogen for Anti-HOXD13 antibody is: synthetic peptide directed towards the N-terminal region of Human HXD13
- Top Product
- Discover our top product HOXD13 Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Antigène
- Homeobox D13 (HOXD13)
- Autre désignation
- HOXD13 (HOXD13 Produits)
- Synonymes
- anticorps XHoxd13, anticorps BDE, anticorps BDSD, anticorps HOX4I, anticorps SPD, anticorps Hox-4.8, anticorps spdh, anticorps hoxd-13, anticorps hoxd13, anticorps zgc:110511, anticorps homeobox D13, anticorps homeobox D13 S homeolog, anticorps homeobox D13a, anticorps homeo box D13, anticorps HOXD13, anticorps hoxd13.S, anticorps Hoxd13, anticorps hoxd13a
- Sujet
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This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.
Alias Symbols: BDE, SPD, BDSD, HOX4I
Protein Size: 343 - ID gène
- 3239
- NCBI Accession
- NP_000514
- UniProt
- P35453
- Pathways
- Synaptic Membrane
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