84-5579-73 ［取扱停止］SEPT9 30ul 542176
特徴
- SEPT9 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.
- Applications:Suitable for use in Western Blot and ELISA.
- Other applications not tested.
- Recommended Dilution:Western Blot: 1:500-1:2000ELISA: 1:5000-1:20,000Optimal dilutions to be determined by the researcher.
- Storage and Stability:May be stored at 4°C for short-term only.
- Aliquot to avoid repeated freezing and thawing.
- Store at -20°C.
- Aliquots are stable for 12 months after receipt.
- For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
- Size：30ul
- Host：rabbit
- Source Antibody：human
- Grade：Affinity Purified
- Purity：Purified by immunoaffinity chromatography.
- Form：Supplied as a liquid in PBS, pH 7.4, 0.02% sodium azide, 50% glycerol.
- Specificity：Recognizes endogenous levels of human SEPT9.
- Isotype：IgG
- Calc Applications Abbrev：E WB
- Calc Crossreactivity：Hu
- Immunogen：Synthetic peptide corresponding to human SEPT9 protein.
- Swiss Prot Number：Q9UHD8
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