84-5041-69 PYGM (Glycogen Phosphorylase, Muscle Form, Phosphorylase, Glycogen, Muscle) 100ul 489830
特徴
- This gene encodes a muscle enzyme involved in glycogenolysis.
- Highly similar enzymes encoded by different genes are found in liver and brain.
- Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle.
- Alternative splicing results in multiple transcript variants.
- Applications:Suitable for use in Western Blot.
- Other applications not tested.
- Recommended Dilution:Optimal 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 affinity chromatography.
- Form:Supplied as a liquid in PBS, 2% sucrose, 0.09% sodium azide.
- Specificity:Recognizes human PYGM.
- Isotype:IgG
- Calc Applications Abbrev:WB
- Calc Crossreactivity:Hu
- Immunogen:Synthetic peptide corresponding to the C-terminal region of human PYGM
- Shelf Life:1year
- Swiss Prot Number:P11217
- EU Commodity Code:30021010
- この商品は法規制を確認しておりません。(法規制によって販売できない場合もございます)
- 製品の仕様は予告なく変更になる場合がございます。最新仕様はメーカーホームページをご確認ください。
- 【試薬に関するお問合せ】
- アズワン株式会社 試薬・プロセス材料グループ
- TEL:06-6447-8641
- FAX:06-6447-8642
- E-mail:[email protected]