AMMECR1 antibody,Genetex,GTX115945
Host
Rabbit
Reactivity
Human
Application
WB ICC/IF
Conjugate
Unconjugated
Platform ID
BAB887154865
Genetex
Contact
Tel: 1-949-553-1900
Fax: 1-949-309-2888
Email:
Product Specifications
Scientific Background
Synonyms
Specifications
NameAMMECR1 antibody
Cat. No.GTX115945
Gene ID (Entrez)9949
HostRabbit
IsotypeIgG
ReactivityHuman
ConjugationUnconjugated
ApplicationWB ICC/IF
ClonalityPolyclonal
Concentration1 mg/ml (Please refer to the vial label for the specific concentration.)
TargetAMMECR1
ImmunogenRecombinant protein encompassing a sequence within the center region of human AMMECR1. The exact sequence is proprietary.
PurityPurified by antigen-affinity chromatography.
Appearance/FormLiquid
Formulation0.1M Tris, 0.1M Glycine, 20% Glycerol,0.01% Thimerosal
StorageStore as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Regulatory StatusResearch Use Only
Scientific Background
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. [provided by RefSeq]
Synonyms
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 , AMMERC1 , MFHIEN
Category Paths
- Products>Primary Antibodies>Polyclonal Antibodies
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