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Espin antibody (AA 585-854)

This anti-Espin antibody is a Rabbit Polyclonal antibody detecting Espin in WB and IHC. Suitable for Human.
Catalog No. ABIN7267008

Quick Overview for Espin antibody (AA 585-854) (ABIN7267008)

Target

See all Espin (ESPN) Antibodies
Espin (ESPN)

Reactivity

  • 20
  • 10
  • 10
Human

Host

  • 21
Rabbit

Clonality

  • 21
Polyclonal

Conjugate

  • 9
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Espin antibody is un-conjugated

Application

  • 13
  • 11
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 8
    • 3
    • 1
    AA 585-854

    Purpose

    ESPN Rabbit pAb

    Sequence

    CAADPKASRE LPPPPPPPPP PLPEAASSPP PAPPLPLESA GPGCGQRRSS SSTGSTKSFN MMSPTGDNSE LLAEIKAGKS LKPTPQSKGL TTVFSGIGQP AFQPDSPLPS VSPALSPVRS PTPPAAGFQP LLNGSLVPVP PTTPAPGVQL DVEALIPTHD EQGRPIPEWK RQVMVRKMQL KMQEEEEQRR KEEEEEARLA SMPAWRRDLL RKKLEEEREQ KRKEEERQKQ EELRREKEQS EKLRTLGYDE SKLAPWQRQV ILKKGDIAKY

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 585-854 of human ESPN (NP_113663.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Espin (ESPN)

    Alternative Name

    ESPN

    Background

    This gene encodes a multifunctional actin-bundling protein. It plays a major role in regulating the organization, dimensions, dynamics, and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in various mechanosensory and chemosensory cells. Mutations in this gene are associated with autosomal recessive neurosensory deafness, and autosomal dominant sensorineural deafness without vestibular involvement.,ESPN,DFNB36,LP2654,espin,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Microfilaments,Neuroscience,ESPN

    Molecular Weight

    31kDa/91kDa

    Gene ID

    83715

    UniProt

    B1AK53

    Pathways

    Sensory Perception of Sound
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