AMMECR1 antibody (C-Term)
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- Target See all AMMECR1 Antibodies
- AMMECR1 (Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 (AMMECR1))
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Binding Specificity
- AA 271-298, C-Term
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This AMMECR1 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purpose
- Rabbit Anti-Human AMMECR1 (C-term) Antibody
- Immunogen
- 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.
- Isotype
- Ig Fraction
- Top Product
- Discover our top product AMMECR1 Primary Antibody
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- Application Notes
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Western Blot
Recommended Dilutions
WB: 1:1000AMMECR1 Antibody (C-term) . - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5 mg/mL
- Storage
- 4 °C,-20 °C
- Storage Comment
- 2-8°C (short-term), -20°C (long-term)
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- Target
- AMMECR1 (Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 (AMMECR1))
- Alternative Name
- AMMECR1 (AMMECR1 Products)
- Synonyms
- ammerc1 antibody, MGC84095 antibody, AMMECR1 antibody, Ammecr1 antibody, AMMERC1 antibody, 6230420G18Rik antibody, Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 L homeolog antibody, Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 antibody, ammecr1.L antibody, AMMECR1 antibody, Ammecr1 antibody, ammecr1 antibody
- Background
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Target Description: 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.
Gene Symbol: AMMECR1
- Molecular Weight
- 35463 Da
- Gene ID
- 9949
- UniProt
- Q9Y4X0
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