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EYA1 antibody (AA 100-250)

The Rabbit Polyclonal anti-EYA1 antibody has been validated for WB and IHC. It is suitable to detect EYA1 in samples from Human.
Catalog No. ABIN6135167

Quick Overview for EYA1 antibody (AA 100-250) (ABIN6135167)

Target

See all EYA1 Antibodies
EYA1 (Eyes Absent Homolog 1 (EYA1))

Reactivity

  • 34
  • 19
  • 8
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
Human

Host

  • 39
  • 1
  • 1
Rabbit

Clonality

  • 41
Polyclonal

Conjugate

  • 18
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EYA1 antibody is un-conjugated

Application

  • 21
  • 18
  • 13
  • 13
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 10
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 100-250

    Sequence

    TPSSQTMAAY GQTQFTTGMQ QATAYATYPQ PGQPYGISSY GALWAGIKTE GGLSQSQSPG QTGFLSYGTS FSTPQPGQAP YSYQMQGSSF TTSSGIYTGN NSLTNSSGFN SSQQDYPSYP SFGQGQYAQY YNSSPYPAHY MTSSNTSPTT P

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 100-250 of human EYA1 (NP_742055.1).

    Isotype

    IgG
  • Application Notes

    WB,1:200 - 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

    EYA1 (Eyes Absent Homolog 1 (EYA1))

    Alternative Name

    EYA1

    Background

    This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Alternatively spliced transcript variants have been identified for this gene.,EYA1,BOP,BOR,BOS1,OFC1,Epigenetics & Nuclear Signaling,Chromatin Modifying Enzymes,Dephosphorylation,Cell Biology & Developmental Biology,EYA1

    Molecular Weight

    60 kDa/61 kDa/64 kDa

    Gene ID

    2138

    UniProt

    Q99502

    Pathways

    Sensory Perception of Sound, Positive Regulation of Response to DNA Damage Stimulus
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