ALMS1 anticorps (AA 1530-1610)

N° du produit ABIN7213562

L’anticorps anti-ALMS1 Polyclonal Lapin est utilisé pour la détection de ALMS1 dans des échantillons de Humain et Souris. Il a été validé pour ELISA, WB, IHC et IF.

Aperçu rapide pour ALMS1 anticorps (AA 1530-1610) (ABIN7213562)

Antigène: ALMS1 (Alstrom Syndrome 1 (ALMS1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALMS1 est non-conjugé

Application: ELISA, Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Détail du produit anti-ALMS1 anticorps

Épitope: AA 1530-1610

Fonction: Rabbit Anti-ALMS1 Polyclonal Antibody

Specificité: ALMS1 Polyclonal Antibody detects endogenous levels of ALMS1 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the Internal region of human ALMS1 at AA range: 1530-1610

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur ALMS1

Antigène: ALMS1 (Alstrom Syndrome 1 (ALMS1))

Autre désignation: ALMS1

Sujet: ALMS1, KIAA0328, Alstrom syndrome protein 1ALMS1 encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein (ALMS1, centrosome and basal body associated protein) functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations ALMS1 cause Alstrom syndrome. There is a pseudogene for ALMS1 located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined.

Poids moléculaire: 460kD

ID gène: 7840

UniProt: Q8TCU4

Pathways: Sensory Perception of Sound, Carbohydrate Homeostasis, M Phase