Actin-Like 7A anticorps (N-Term)

N° du produit ABIN654426

Cet anticorps anti-Actin-Like 7A est un anticorps Lapin Polyclonal détectant Actin-Like 7A dans WB. Adapté pour Humain.

Aperçu rapide pour Actin-Like 7A anticorps (N-Term) (ABIN654426)

Antigène: Actin-Like 7A (ACTL7A)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Actin-Like 7A est non-conjugé

Application: Western Blotting (WB)

Clone: RB22393

Détail du produit anti-Actin-Like 7A anticorps

Épitope: AA 41-67, N-Term

Homologie: Pr

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

Immunogène: This ACTL7A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 41-67 amino acids from the N-terminal region of human ACTL7A.

Isotype: Ig Fraction

Information d'application

Indications d'application: 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: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Actin-Like 7A

Antigène: Actin-Like 7A (ACTL7A)

Autre désignation: ACTL7A

Sujet: ACTL7A is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. ACTL7A (ACTL7A), and related gene, ACTL7B, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7A gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. The ACTL7A gene is expressed in a wide variety of adult tissues, however, its exact function is not known.

Poids moléculaire: 48644

ID gène: 10881

NCBI Accession: NP_006678

UniProt: Q9Y615