Septin 9 Protein (SEPT9) (Transcript Variant 7) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2731699

Produktdetails

Target: Septin 9 (SEPT9)

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 7

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses Septin 9 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human Septin-9 (SEPT9) (transcript variant 7) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: Septin 9 (SEPT9)

Andere Bezeichnung: Septin-9 (Sept9) (SEPT9 Produkte)

Synonyme: SEPT9 Protein, msf Protein, msf1 Protein, napb Protein, sint1 Protein, pnutl4 Protein, septd1 Protein, af17q25 Protein, septin-9 Protein, AF17q25 Protein, MSF Protein, MSF1 Protein, NAPB Protein, PNUTL4 Protein, SINT1 Protein, SeptD1 Protein, Msf Protein, Sint1 Protein, Eseptin Protein, Slpa Protein, cb999 Protein, fb02h06 Protein, sept9 Protein, wu:fb02h06 Protein, septin 9 Protein, septin-9 Protein, septin 9 S homeolog Protein, septin 9a Protein, SEPT9 Protein, sept9 Protein, LOC100605286 Protein, sept9.S Protein, Sept9 Protein, sept9a Protein

Hintergrund: 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].

Molekulargewicht: 38.3 kDa

NCBI Accession: NP_001106968