FXR2 Antibodies

AND FXR2 ELISA kits, FXR2 Proteins

Many biological assays use antibodies to detect FXR2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with FXR2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop FXR2 antibodies...

We validate the specificity of these antibodies to FXR2 by testing them on tissues known to express FXR2 positively and negatively. Browse below to find the FXR2 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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FXR2 Infographic by Boster Bio

All FXR2 Products

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Specificity

Applications

Price

Anti-FXR2 (E576) Antibody

Human, Mouse, Rat

IP, IF, IHC, WB

$405
Cat # A05130
100ul

Anti-FXR2 Antibody Picoband®

Human, Monkey, Mouse

ELISA, Flow Cytometry, WB

$370
Cat # A05130-4
100 μg/vial

FXR2 Overview

Facts about Fragile X mental retardation syndrome-related protein 2.

FXR2 3D structure. Source: alphafold

Fragile X mental retardation syndrome-related protein 2 (FXR2)

RNA-binding protein. .

Gene Information

Human
Gene Name:	FXR2
Uniprot:	P51116
Entrez:	9513

Family

Belongs to:

FMR1 family

Alternative Names

FMR1L2; fragile X mental retardation syndrome-related protein 2; fragile X mental retardation, autosomal homolog 2; fragile X-mental retardation 1-like 2; FXR2P

Molecular Weight

Mass (kDA):
74.223 kDA

Genomic Context


Human

Location:	17p13.1
Sequence:	17; NC_000017.11 (7591230..7614897, complement)

Subcellular Localizations

Cytoplasm.

Diseases

Fragile X Syndrome
Nervousness
Trinucleotide Repeat Expansion
Malignant Neoplasms
Neoplasms
Autistic Disorder
Impairment (finding)
Spinal And Bulbar Muscular Atrophy, X-linked 1
Malnutrition
Premature Menopause
Congenital Anomaly Of Face

Fraxe Syndrome
Memory Impairment
Lymphoma
Cell Transformation, Neoplastic
Anxiety Disorders
Congenital Abnormality

Interacting Proteins

AP1M1
ARL6IP1
BYSL
C10orf62
CAMK2D

CDKL3
CEP44
CEP55
FAM90A1
HMBOX1

LASP1
LCMT1
LCP2
LDOC1
MBIP

MCRS1
MEAF6
MFAP1
MMTAG2
MORF4L1

MRPL43
NIF3L1
NT5C2
PAF1
PAICS

PCBD1
PIM1
POM121
PRAM1
RABAC1

SCEL
SRPK2
SYTL4
TBC1D22B
YES1

ZBTB22
ZMAT2

Pathways

Localization
Translation
Pathogenesis
Transport
Nuclear Export
Prepulse Inhibition
Intracellular Transport
Neurogenesis
Synaptic Transmission
Mrna Transport
Spermatogenesis
Methylation

Startle Response
Circadian Behavior
System Development
Cell Cycle
Nervous System Development
Regulation Of Translation

PTMs

Methylation

Phosphorylation

Acetylation

Research Areas

Cellular Markers
Chromatin Research
Neurodegeneration
Neuroscience

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/FXR2

References

PMID: 7489725 by Zhang Y., et al. The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.

PMID: 9437788 by Joseph D.R.; The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: evidence that the ABP/SHBG and the fragile X-related 2 genes overlap.