84-3665-45　［取扱停止］FKTN (Fukutin, Fukuyama-type Congenital Muscular Dystrophy Protein, FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4, MGC126857, MGC134944, MGC134945, MGC138243) (AP) 100ul　137979-AP

特徴

• FKTN regulates the migration and assembly of neurons during cortical histogenesis.
• Fukuyama congenital muscular dystrophy results from mutations in its gene.
• Applications:Suitable for use in Western Blot and Immunohistochemistry.
• Other applications not tested.
• Recommended Dilution:Western Blot: 5ug/mlImmunohistochemistry: 4-8ug/mlOptimal dilutions to be determined by the researcher.
• Storage and Stability:Store product at 4°C.
• DO NOT FREEZE! Stable at 4°C for 12 months after receipt as an undiluted liquid.
• Dilute required amount only prior to immediate use.
• Further dilutions can be made in assay buffer.
• For maximum recovery of product, centrifuge the original vial prior to removing the cap.
• Note: Applications are based on unconjugated antibody.

仕様

• Size：100ul
• Host：rabbit
• Source Antibody：human
• Grade：Affinity Purified
• Purity：Purified by Protein A affinity chromatography.
• Form：Supplied as a liquid in PBS, pH 7.2. No preservative added. Labeled with Alkaline Phosphatase (AP).
• Specificity：Recognizes FKTN. Species Crossreactivity: Human, rat, and canine.
• Isotype：IgG
• Calc Applications Abbrev：IHC WB
• Calc Crossreactivity：Ca Hu Rt
• Immunogen：N-terminus of FKTN corresponding to TAFALQYHLWKNEEGWFRIAENMGFQCLKIESKDPRLDGIDSLSGTEIPL
• Shelf Life：1year
• EU Commodity Code：30021010
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