Homeobox D13 Antikörper (N-Term)

Produktnummer ABIN5516975

Dieses Anti-Homeobox D13-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Homeobox D13 in WB. Geeignet für Human.

Kurzübersicht für Homeobox D13 Antikörper (N-Term) (ABIN5516975)

Target: Homeobox D13 (HOXD13)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Homeobox D13 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-Homeobox D13 Antikörper

Bindungsspezifität: N-Term

Sequenz: ASGFAYPGTS ERTGSSSSSS SSAVVAARPE APPAKECPAP TPAAAAAAPP

Produktmerkmale: This is a rabbit polyclonal antibody against HXD13. It was validated on Western Blot.

Aufreinigung: Affinity purified

Immunogen: The immunogen for Anti-HOXD13 antibody is: synthetic peptide directed towards the N-terminal region of Human HXD13

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu Homeobox D13

Target: Homeobox D13 (HOXD13)

Andere Bezeichnung: HOXD13

Hintergrund: This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.

Alias Symbols: BDE, SPD, BDSD, HOX4I

Protein Size: 343

Gen-ID: 3239

NCBI Accession: NP_000514

UniProt: P35453

Pathways: Synaptic Membrane