AMMECR1 anticorps (C-Term)
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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, C-Term
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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 non-conjugé
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Application
- Western Blotting (WB)
- Homologie
- M
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- 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.
- Clone
- RB39848
- Isotype
- Ig Fraction
- Top Product
- Discover our top product AMMECR1 Anticorps primaire
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- Indications d'application
- WB: 1:1000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- AMMECR1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
- 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
- The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
- Poids moléculaire
- 35463
- ID gène
- 9949
- NCBI Accession
- NP_001020751, NP_001165160, NP_056180
- UniProt
- Q9Y4X0
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