Homeobox D13 anticorps (Middle Region)

N° du produit ABIN952786

Cet anticorps Lapin Polyclonal détecte spécifiquement Homeobox D13 dans WB et EIA. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour Homeobox D13 anticorps (Middle Region) (ABIN952786)

Antigène: Homeobox D13 (HOXD13)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Homeobox D13 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-Homeobox D13 anticorps

Épitope: AA 201-230, Middle Region

Specificité: This antibody recognizes Human and Mouse HOXD13 / HOX4I (C-term).

Purification: Protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 201-230 amino acids from the Central region of human HOXD13 / HOX4I

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur Homeobox D13

Antigène: Homeobox D13 (HOXD13)

Autre désignation: HOXD13 / HOX4I

Sujet: 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.Synonyms: Homeobox protein Hox-D13, Hox-4I

Poids moléculaire: 36101 Da

ID gène: 3239

NCBI Accession: NP_000514

Pathways: Synaptic Membrane