84-1150-50 PFKM, NT (6-phosphofructokinase, Muscle Type, Phosphofructokinase 1, Phosphohexokinase, Phosphofructo-1-kinase Isozyme A, PFK-A, Phosphofructokinase-M, PFKX) 200ul F8060-06A
特徴
- Phosphofructokinase catalyzes the irreversible conversion of fructose 6 phosphate to fructose 1,6 bisphosphate.
- Mammalian PFK is a complex isozyme consisting of 3 subunits: muscle (M), liver (L), and platelet (P).
- Only M type PFK isozyme is expressed in mature muscle, while erythrocytes contain both L and M subunits.
- Defects in PFKM are the cause of glycogen storage disease type 7 (GSD7), also known as Tarui disease.
- Applications:Suitable for use in ELISA, Western Blot, and Immunohistochemistry.
- Other applications not tested.
- Recommended Dilution:ELISA: 1:1,000Western Blot: 1:100-1:500Immunohistochemistry: 1:50-1:100Optimal 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 at least 12 months.
- For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
- Size：200ul
- Host：rabbit
- Source Antibody：human
- Grade：Affinity Purified
- Purity：Purified by Protein G affinity chromatography.
- Form：Supplied as a liquid in PBS, 0.09% sodium azide.
- Specificity：Recognizes human PFKM.
- Isotype：IgG
- Calc Applications Abbrev：E IHC WB
- Calc Crossreactivity：Hu
- Immunogen：Synthetic peptide selected from the N-terminal region of human PFKM (KLH).
- Shelf Life：1year
- Swiss Prot Number：P08237
- EU Commodity Code：30021010
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