HOXD10 anticorps (AA 111-210)

N° du produit ABIN6988988

L’anticorps Lapin Polyclonal anti-HOXD10 a été validé pour IHC (p) et IHC (fro). Il convient pour détecter HOXD10 dans des échantillons de Rat.

Aperçu rapide pour HOXD10 anticorps (AA 111-210) (ABIN6988988)

Antigène: HOXD10 (Homeobox D10 (HOXD10))

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HOXD10 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-HOXD10 anticorps

Épitope: AA 111-210

Réactivité croisée: Rat

Homologie: Human,Mouse,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human HOXD10

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur HOXD10

Antigène: HOXD10 (Homeobox D10 (HOXD10))

Autre désignation: HOXD10

Sujet:

Synonyms: Homeo box D10, Homeobox protein Hox-4D, Homeobox protein Hox-4E, Homeobox protein Hox-D10, Hox 4.5, Hox 4D, Hox 4E, HOX4D, HOXD10, HXD10, HXD10_HUMAN, Hox 5.3.

Background: 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. [provided by RefSeq, Jul 2008]

ID gène: 3236

UniProt: P28358