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Human FMR1 ELISA Kit

CAT: 0013-GTR18815989-01Size: 24 TestsDry Ice: NoHazardous: No
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CAT#:0013-GTR18815989-01Size:24 Tests
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Description
The Human FMR1 ELISA Kit detects the target FMR1 in human samples. It measures levels in sample types including serum, plasma and tissue homogenates. The detection range is 15.6 pg/mL-1000 pg/mL. The kit offers a sensitivity of 3.9 pg/mL.
Product Name Alternative
FMR 1 ELISA Kit; Fmr1 ELISA Kit; Fmr1 gene ELISA Kit; FMR1_HUMAN ELISA Kit; FMRP ELISA Kit; Fragile X mental retardation 1 ELISA Kit; Fragile X mental retardation 1 protein ELISA Kit; Fragile X mental retardation protein 1 ELISA Kit; Fragile X mental retardation protein ELISA Kit; fragile X mental retardation syndrome-related protein 1 ELISA Kit; fragile X mental retardation; autosomal homolog 1 ELISA Kit; FRAXA ELISA Kit; fxr1 ELISA Kit; MGC87458 ELISA Kit; POF ELISA Kit; POF1 ELISA Kit; Protein FMR-1 ELISA Kit; Protein FMR1 ELISA Kit; wu:fb16f11 ELISA Kit; wu:fd18c10 ELISA Kit; zgc:66226 ELISA Kit
UniProt
Q06787
Reactivity
Human
Target
FMR1
Field of Research
Neuroscience
Assay Type
Sandwich
Assay Performance Time
1-5h
Sample Type
Serum, plasma, tissue homogenates
Sensitivity
3.9 pg/mL
Notes
For research use only.
Applications Notes
Detection Wavelength: 450 nm
Dynamic Range
15.6 pg/mL-1000 pg/mL

UniProtKB · Q06787

Fragile X messenger ribonucleoprotein 1

FMR1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q06787
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
FMR1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A6NNH4, D3DWT0, D3DWT1, D3DWT2, G8JL90, Q16578, Q5PQZ6, Q99054
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationMethylationPhosphoproteinUbl conjugation

Molecular function

ActivatorRepressorRibonucleoproteinRNA-binding

Coding sequence diversity

Alternative splicing

Cellular component

Cell membraneCell projectionCentromereChromosomeCytoplasmMembraneNucleusPostsynaptic cell membraneSynapseSynaptosome

Disease

Disease variantIntellectual disabilityNeurodegenerationPremature ovarian failure

Biological process

DNA damageHost-virus interactionmRNA processingmRNA splicingmRNA transportNeurogenesisRNA-mediated gene silencingTranslation regulationTransport

Domain

Repeat

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