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ELMOD3 antibody (AA 290-381)

This Rabbit Polyclonal antibody specifically detects ELMOD3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7266922

Quick Overview for ELMOD3 antibody (AA 290-381) (ABIN7266922)

Target

See all ELMOD3 Antibodies
ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))

Reactivity

  • 14
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 11
  • 3
Rabbit

Clonality

  • 14
Polyclonal

Conjugate

  • 10
  • 2
  • 1
  • 1
This ELMOD3 antibody is un-conjugated

Application

  • 10
  • 6
  • 5
  • 2
Western Blotting (WB)
  • Binding Specificity

    • 6
    • 2
    • 2
    • 1
    AA 290-381

    Purpose

    ELMOD3 Rabbit pAb

    Sequence

    ATFLHLAHVW RTQRKTISDS GFVLKELEVL AKKSPRRLLK TLELYLARVS KGQASLLGAQ KCYGPEAPPF KDLTFTGESD LQSHSSEGVW LI

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 290-381 of human ELMOD3 (NP_001128493.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    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

    ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))

    Alternative Name

    ELMOD3

    Background

    This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants.,ELMOD3,DFNB88,LST3,RBED1,RBM29,Signal Transduction,G protein signaling,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Endocrine & Metabolism,ELMOD3

    Molecular Weight

    18kDa/20kDa/28kDa/43kDa/44kDa

    Gene ID

    84173

    UniProt

    Q96FG2
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