ALMS1 Antikörper (AA 1530-1610)

Produktnummer ABIN7213562

Der Kaninchen Polyklonal anti-ALMS1 Antikörper wird verwendet zum Nachweis von ALMS1 in Proben von Human und Maus. Er wurde validiert für ELISA, WB, IHC und IF.

Kurzübersicht für ALMS1 Antikörper (AA 1530-1610) (ABIN7213562)

Target: ALMS1 (Alstrom Syndrome 1 (ALMS1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALMS1 Antikörper ist unkonjugiert

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

Produktdetails anti-ALMS1 Antikörper

Bindungsspezifität: AA 1530-1610

Verwendungszweck: Rabbit Anti-ALMS1 Polyclonal Antibody

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

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

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: 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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 12 months

Details zu ALMS1

Target: ALMS1 (Alstrom Syndrome 1 (ALMS1))

Andere Bezeichnung: ALMS1

Hintergrund: 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.

Molekulargewicht: 460kD

Gen-ID: 7840

UniProt: Q8TCU4

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