SALL1 Antikörper

Produktnummer ABIN7231246

Der Kaninchen Polyklonal anti-SALL1 Antikörper wird verwendet zum Nachweis von SALL1 in Proben von Human und Maus. Er wurde validiert für WB und ELISA.

Kurzübersicht für SALL1 Antikörper (ABIN7231246)

Target: SALL1 (Sal-Like 1 (SALL1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SALL1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-SALL1 Antikörper

Verwendungszweck: Rabbit Anti-SALL1 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of SALL1 protein

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

Immunogen: Synthesized peptide derived from part region of human SALL1 protein

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: 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 SALL1

Target: SALL1 (Sal-Like 1 (SALL1))

Andere Bezeichnung: SALL1

Hintergrund: Sal-like protein 1, Spalt-like transcription factor 1, Zinc finger protein 794, Zinc finger protein SALL1, Zinc finger protein Spalt-1, HSal1Spalt Like Transcription Factor 1 encoded by SALL1 is a zinc finger transcriptional repressor and may be part of the NuRD histone deacetylase complex (HDAC). Defects in this gene are a cause of Townes-Brocks syndrome (TBS) as well as bronchio-oto-renal syndrome (BOR). Two transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht: 145kD

Gen-ID: 6299

UniProt: Q9NSC2

Pathways: Tube Formation