ANKS3 anticorps

N° du produit ABIN1386930

Cet anticorps anti-ANKS3 est un anticorps Lapin Polyclonal détectant ANKS3 dans IF (p) et IHC (p). Adapté pour Humain, Souris et Rat.

Aperçu rapide pour ANKS3 anticorps (ABIN1386930)

Antigène: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ANKS3 est non-conjugé

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

Détail du produit anti-ANKS3 anticorps

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ANKS3

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IF(IHC-P) 1:50-200

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 ANKS3

Antigène: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Autre désignation: ANKS3

Sujet:

Synonyms: Ankyrin repeat and SAM domain containing protein 3, Ankyrin repeat and sterile alpha mot domain containing 3, KIAA1977, ANKS3_HUMAN.

Background: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

ID gène: 124401