Homeobox D13 Antikörper (AA 202-230)

Produktnummer ABIN655171

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Homeobox D13 in WB. Er zeigt eine Reaktivität gegenüber Maus.

Kurzübersicht für Homeobox D13 Antikörper (AA 202-230) (ABIN655171)

Target: Homeobox D13 (HOXD13)

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Homeobox D13 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: RB19191

Produktdetails anti-Homeobox D13 Antikörper

Bindungsspezifität: AA 202-230

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This HOXD13 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 202-230 amino acids from the Central region of human HOXD13.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Informationen zur Lagerung: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Haltbarkeit: 6 months

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.

Molekulargewicht: 36101

Gen-ID: 3239

NCBI Accession: NP_000514

UniProt: P35453

Pathways: Synaptic Membrane