HOXD10 anticorps (C-Term)

N° du produit ABIN656539

Cet anticorps Lapin Polyclonal détecte spécifiquement HOXD10 dans WB. Il présente une réactivité envers Souris et Poisson zèbre (Danio rerio).

Aperçu rapide pour HOXD10 anticorps (C-Term) (ABIN656539)

Antigène: HOXD10 (Homeobox D10 (HOXD10))

Reactivité: Souris, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HOXD10 est non-conjugé

Application: Western Blotting (WB)

Clone: RB32058

Détail du produit anti-HOXD10 anticorps

Épitope: AA 305-334, C-Term

Homologie: C

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This HOXD10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 305-334 amino acids from the C-terminal region of human HOXD10.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: HOXD10 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Date de péremption: 6 months

Détails sur HOXD10

Antigène: HOXD10 (Homeobox D10 (HOXD10))

Autre désignation: HOXD10

Sujet: This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as 'rocker-bottom foot' deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease.

Poids moléculaire: 38411

ID gène: 3236

NCBI Accession: NP_002139

UniProt: P28358