產品詳情
簡單介紹:
AMME Syndrome Candidate Gene 1 Protein (AMMECR1) Antibody
詳情介紹:
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.
Research Articles on AMME Syndrome Candidate Gene 1 Protein (AMMECR1)
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. |
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