HMGN1 anticorps (AA 90-100)

N° du produit ABIN7448975

L’anticorps anti-HMGN1 Polyclonal Lapin est utilisé pour la détection de HMGN1 dans des échantillons de Humain et Souris. Il a été validé pour IHC et IF (p).

Aperçu rapide pour HMGN1 anticorps (AA 90-100) (ABIN7448975)

Antigène: HMGN1 (High Mobility Group Nucleosome Binding Domain 1 (HMGN1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HMGN1 est non-conjugé

Application: Immunohistochemistry (IHC), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-HMGN1 anticorps

Épitope: AA 90-100

Fonction: Rabbit anti-HMGN1 IHC Antibody, Affinity Purified

Homologie: Dog,Horse,Pig,Panda,Orangutan,Monkey,Gorilla,Chimpanzee,Crab-eating macaque,Olive baboon,White-tufted-ear marmoset,Northern white-cheeked gibbon,Dusky titi monkey,Small-eared galago

Purification: Affinity Purified

Immunogène: Between AA 90 and 100

Isotype: IgG

Information d'application

Indications d'application:

IHC-IF: 1:50 - 1:500

IHC: 1:100 - 1:500

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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

Date de péremption: 12 months

Détails sur HMGN1

Antigène: HMGN1 (High Mobility Group Nucleosome Binding Domain 1 (HMGN1))

Autre désignation: HMGN1

Sujet: Background: HMGN1 and its close analog HMG17 (MIM 163910) bind to the inner side of the nucleosomal DNA to potentially alter the interaction between the DNA and the histone octamer. The two proteins may be involved in the process that maintains transcribable genes in a unique chromatin conformation. Their ubiquitous distribution and relative abundance, as well as the high evolutionary conservation of the DNA-binding domain of the HMG14 family of proteins, suggest that they may be involved in an important cellular function [taken from NCBI Entrez Gene (GeneID:3150)].

ID gène: 3150

NCBI Accession: NP_004956

UniProt: P05114

Pathways: Chromatin Binding