MSF (SEPT9) (NM_001113496) Human Recombinant Protein
Product Specifications
Background
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]
Synonyms
AF17q25; MSF; MSF1; NAPB; PNUTL4; SEPT9; SeptD1; SINT1
Gene ID
10801
UniProt
Q9UHD8
Accession Number mRNA
NM_001113496
Chromosomal Location
17q25.3
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome
Molecular Weight
38.3 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
SEPTIN9
Species
Human
Protein ID
NP_001106968
Overview
Purified recombinant protein of Homo sapiens septin 9 (SEPT9), transcript variant 7
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/10801
Uniprot URL
https://www.uniprot.org/uniprot/Q9UHD8
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001113496
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001106968
Curated Selection
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