AMME Syndrome Candidate Gene 1 Protein (AMMECR1) Antibody

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Catalogue No: abx030753
Price: US$326.25
(Size: 80 µl)

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Datasheet SDS
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.

Target AMME Syndrome Candidate Gene 1 Protein (AMMECR1)
Clonality Polyclonal
Reactivity Human
Tested Applications ELISA, WB
Host Rabbit
Recommended dilutions WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 271-298 amino acids from the C-terminal region of human AMMECR1.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC Q9Y4X0 (UniProt, ExPASy)
UniProt Secondary AC Q5JYV9, Q6P9D8, Q8WX22, Q9UIQ8
UniProt Entry Name AMMR1_HUMAN
Gene Symbol AMMECR1
String 9606.ENSP00000262844
Molecular Weight Calculated MW: 35.5 kDa
Buffer PBS containing 0.09% sodium azide.
Specificity Predicted to react with Mouse AMMECR1.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on AMME Syndrome Candidate Gene 1 Protein (AMMECR1)


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