AMMECR1 anticorps (AA 271-298) (APC)
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- Antigène Voir toutes AMMECR1 Anticorps
- AMMECR1 (Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 (AMMECR1))
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Épitope
- AA 271-298
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp AMMECR1 est conjugé à/à la APC
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Application
- ELISA, Western Blotting (WB)
- Specificité
- This AMMECR1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 271-298 amino acids from the C-terminal region of human AMMECR1.
- Purification
- Affinity purified
- Isotype
- IgG
- Top Product
- Discover our top product AMMECR1 Anticorps primaire
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- Indications d'application
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Approved: ELISA, WB
Usage: The applications listed have been tested for the unconjugated form of this product. Other forms have not been tested. - Commentaires
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Target Species of Antibody: Human
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- PBS, no preservatives added
- Agent conservateur
- Without preservative
- Conseil sur la manipulation
- Aliquot to avoid repeated freezing and thawing.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Short term: store at 4°C. Long term: aliquot and store -20°C for up to 6 months. Avoid freeze-thaw cycles. Protect from light.
- Date de péremption
- 6 months
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- Antigène
- AMMECR1 (Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 (AMMECR1))
- Autre désignation
- AMMECR1 (AMMECR1 Produits)
- Synonymes
- anticorps ammerc1, anticorps MGC84095, anticorps AMMECR1, anticorps Ammecr1, anticorps AMMERC1, anticorps 6230420G18Rik, anticorps Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 L homeolog, anticorps Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1, anticorps ammecr1.L, anticorps AMMECR1, anticorps Ammecr1, anticorps ammecr1
- Sujet
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Name/Gene ID: AMMECR1
Synonyms: AMMECR1, AMMERC1 - ID gène
- 9949
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