Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

FMR1 antibody

This anti-FMR1 antibody is a Rabbit Polyclonal antibody detecting FMR1 in WB, IHC, ELISA, IF and IP. Suitable for Human, Mouse and Rat.
Catalog No. ABIN5697696

Quick Overview for FMR1 antibody (ABIN5697696)

Target

See all FMR1 Antibodies
FMR1 (Fragile X Mental Retardation 1 (FMR1))

Reactivity

  • 77
  • 54
  • 43
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 62
  • 19
  • 2
Rabbit

Clonality

  • 55
  • 28
Polyclonal

Conjugate

  • 50
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FMR1 antibody is un-conjugated

Application

  • 68
  • 24
  • 22
  • 15
  • 14
  • 13
  • 11
  • 10
  • 9
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Immunogen

    fragile X mental retardation 1

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    K-562 cells were subjected to SDS PAGE followed by western blot with FNab03172(FMR1 antibody) at dilution of 1:500

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Expiry Date

    12 months
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Alternative Name

    FMR1

    Background

    Synonyms:FMRP Background:The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene.

    Gene ID

    2332

    UniProt

    Q06787

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
You are here:
Chat with us!