Homeobox D13 Antikörper (Middle Region)

Produktnummer ABIN952786

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

Kurzübersicht für Homeobox D13 Antikörper (Middle Region) (ABIN952786)

Target: Homeobox D13 (HOXD13)

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Homeobox D13 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Produktdetails anti-Homeobox D13 Antikörper

Bindungsspezifität: AA 201-230, Middle Region

Spezifität: This antibody recognizes Human and Mouse HOXD13 / HOX4I (C-term).

Aufreinigung: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 201-230 amino acids from the Central region of human HOXD13 / HOX4I

Isotyp: Ig Fraction

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu Homeobox D13

Target: Homeobox D13 (HOXD13)

Andere Bezeichnung: HOXD13 / HOX4I

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.Synonyms: Homeobox protein Hox-D13, Hox-4I

Molekulargewicht: 36101 Da

Gen-ID: 3239

NCBI Accession: NP_000514

Pathways: Synaptic Membrane