SEPTIN9抗体;SEPTIN9 Polyclonal A

Description This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009] Specification Aliases:MSF; MSF1; NAPB; SEPT9; SINT1; PNUTL4; SeptD1; AF17q25 Swissprot:Q9UHD8 Host/Isotype:Rabbit IgG Antibody Type:Primary antibody Storage:Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. Species Reactivity:Human, Mouse, Rat Immunogen:Fusion protein of human SEPTIN9 Formulation:pH7.4 PBS, 0.05% NaN3, 40% Glycerol Application IHC:1/15-1/50 ELISA:1/1000-1/2000