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Acetylcholine receptor protein, epsilon subunit precursor (CHRNE) antibody
Acetylcholine receptor protein, epsilon subunit precursor
Acetylcholine receptor subunit epsilon
Gene name: CHRNE, ACHRE
Acetylcholine receptor subunit epsilon
Gene name: CHRNE, ACHRE
As low as
$306.10
In stock
Ref
00013562
Belongs to the ligand-gated ion channel family. Acetylcholine receptor subfamily. Epsilon/CHRNE sub-subfamily.
Defects in CHRNE are a cause of congenital myasthenic syndrome slow-channel type (SCCMS), congenital myasthenic syndrome fast-channel type (FCCMS) and congenital myasthenic syndrome with acetylcholine receptor deficiency (CMS-ACHRD).
Defects in CHRNE are a cause of congenital myasthenic syndrome slow-channel type (SCCMS), congenital myasthenic syndrome fast-channel type (FCCMS) and congenital myasthenic syndrome with acetylcholine receptor deficiency (CMS-ACHRD).
ID Covalab | pab0265 |
---|---|
Product type | Primary antibodies |
Clonality | Polyclonal antibody |
Raised in | Rabbit |
Immunogen | Synthetic peptide derived from the human CHRNE protein. |
Activity cross reaction | Reacts with human and mouse CHRNE protein. May cross reacts with protein from rat and other species due to sequence homology (> 80%). |
Species | Hu, Ms |
Labelling | None |
Form | Antiserum |
Preservative | None |
Storage instructions | Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt. |
Target | Acetylcholine receptor protein, epsilon subunit precursor (CHRNE) |
Uniprot ID | Q04844 |
Gene ID | 1145 |
Applications | ELISA, IF, WB |
Working dilutions | Optimal dilution should be determined by the end user. The following are guidelines only : IF (1:200 - 1:1000) WB (1:500 - 1:5000) |
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