84-5401-79 ［取扱停止］AFG3L2 100ul 532821
特徴
- AFG3L2 (AFG3 Like Matrix AAA Peptidase Subunit 2) is a Protein Coding gene.
- Diseases associated with AFG3L2 include Spinocerebellar Ataxia 28 and Spastic Ataxia 5, Autosomal Recessive.
- AFG3L2 encodes a protein localized in mitochondria and closely related to paraplegin.
- The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia.
- AFG3L2 is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
- Applications:Suitable for use in Western Blot and ELISA.
- Other applications not tested.
- Recommended Dilution:Western Blot: 1:500-1:2000ELISA: 1:10,000-1:20,000Optimal 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：100ul
- 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 AFG3L2.
- Isotype：IgG
- Calc Applications Abbrev：E WB
- Calc Crossreactivity：Hu
- Immunogen：Synthetic peptide corresponding to aa744-793 from human AFG3L2.
- Swiss Prot Number：Q9Y4W6
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