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FMR1 Antibody (N-term)

CAT: 0013-GTR18327184-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18327184-01Size:50 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Affinity Purified Rabbit Polyclonal Antibody (Pab)
Product Name Alternative
Fragile X mental retardation protein 1, FMRP, Protein FMR-1, FMR1
UniProt
Q06787
Reactivity
Human, Mouse
Immunogen
This FMR1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 20-48 amino acids from the N-terminal region of human FMR1. Antigen Region: 20-48 aa.
Target
FMR1 {ECO:0000303|PubMed:8504300, ECO:0000312|HGNC:HGNC:3775}
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Dilution
WB - 1:1000, IHC-P - 1:50-100, FC - 1:10-50
Form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Molecular Weight
71174 Da
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Notes
For research use only.
Tested Applications
FC, IHC-P, WB
NCBI Accession Number
NP_001172005.1, NP_002015.1, NP_001172004.1, NP_001172010.1, NP_001172011.1
Host or Source
Rabbit
Isotype
Rabbit IgG

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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