HMX2 Antikörper

Produktnummer ABIN7228944

Der Kaninchen Polyklonal anti-HMX2 Antikörper wird verwendet zum Nachweis von HMX2 in Proben von Human und Maus. Er wurde validiert für WB und ELISA.

Kurzübersicht für HMX2 Antikörper (ABIN7228944)

Target: HMX2 (H6 Family Homeobox 2 (HMX2))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HMX2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-HMX2 Antikörper

Verwendungszweck: Rabbit Anti-HMX2 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of HMX2 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 HMX2 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 HMX2

Target: HMX2 (H6 Family Homeobox 2 (HMX2))

Andere Bezeichnung: HMX2

Hintergrund: Homeobox protein HMX2, Homeobox protein H6 family member 2The protein encoded by HMX2 is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing HMX2 have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. HMX2 (H6 Family Homeobox 2) is a Protein Coding gene. Diseases associated with HMX2 include Cecal Benign Neoplasm and Cecum Adenocarcinoma.

Molekulargewicht: 30kD

Gen-ID: 3167

UniProt: A2RU54