MSX1 anticorps (AA 111-138)

N° du produit ABIN1537757

L’anticorps Lapin Polyclonal anti-MSX1 a été validé pour WB et IF. Il convient pour détecter MSX1 dans des échantillons de Humain et Souris.

Aperçu rapide pour MSX1 anticorps (AA 111-138) (ABIN1537757)

Antigène: MSX1 (Msh Homeobox 1 (MSX1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MSX1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Clone: RB30384

Détail du produit anti-MSX1 anticorps

Épitope: AA 111-138

Homologie: B

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

Immunogène: This MSX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 111-138 amino acids from the Central region of human MSX1.

Isotype: Ig Fraction

Information d'application

Indications d'application: IF: 1:10~50. IF: 1:200. WB: 1:1000. WB: 1:2000. 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: MSX1 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur MSX1

Antigène: MSX1 (Msh Homeobox 1 (MSX1))

Autre désignation: MSX1

Sujet: This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.

Poids moléculaire: 31496

ID gène: 4487

NCBI Accession: NP_002439

UniProt: P28360

Pathways: Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus