MSF (SEPT9) Mouse Monoclonal Antibody [Kloon ID: LBI13B1]

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]

Carrier-free (BSA/glycerol-free) SEPT9 mouse monoclonal antibody, clone LBI13B1

AF17q25; MSF; MSF1; NAPB; PNUTL4; SEPT9; SeptD1; SINT1

Homo sapiens septin 9 (SEPTIN9), transcript variant 3, mRNA.

10801

Q9UHD8

Unconjugated

WB 1:500~2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

SEPTIN9

https://www.ncbi.nlm.nih.gov/gene/?term=10801

https://www.uniprot.org/uniprot/Q9UHD8