84-5358-13 ［取扱停止］KAL1 100ul 530933
特徴
- Mutations in this gene cause the X-linked Kallmann syndrome.
- The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration.
- In addition, this cell surface protein is N-glycosylated and may have anti-protease activity.
- Applications:Suitable for use in Western Blot and Immunofluorescence.
- Other applications not tested.
- Recommended Dilution:Western Blot: 1:500-1:2000Immunofluorescence: 1:50-1:200Optimal dilutions to be determined by the researcher.
- AA Sequence:LEVKWSSKFNISIEPVIYVVQRRWNYGIHPSEDDATHWQTVAQTTDERVQLTDIRPSRWYQFRVAAVNVHGTRGFTAPSKHFRSSKDPSAPPAPANLRLAN
- 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：100ul
- Host：rabbit
- Source Antibody：human
- Grade：Affinity Purified
- Purity：Purified by affinity chromatography.
- Form：Supplied as a liquid in PBS, pH 7.3, 0.02% sodium azide, 50% glycerol.
- Specificity：Recognizes human KAL1. Species Crossreactivity: mouse
- Isotype：IgG
- Calc Applications Abbrev：IF WB
- Calc Crossreactivity：Hu Mo
- Immunogen：Synthetic peptide corresponding to a sequence within aa200-300 of human KAL1 (NP_000207.2).
- Swiss Prot Number：P23352
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