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KLHL3 antibody (AA 1-110)

This Rabbit Polyclonal antibody specifically detects KLHL3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN6142937

Quick Overview for KLHL3 antibody (AA 1-110) (ABIN6142937)

Target

See all KLHL3 Antibodies
KLHL3 (Kelch-Like 3 (KLHL3))

Reactivity

  • 50
  • 9
  • 8
  • 8
  • 8
  • 7
  • 6
  • 6
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 48
  • 2
Rabbit

Clonality

  • 50
Polyclonal

Conjugate

  • 21
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KLHL3 antibody is un-conjugated

Application

  • 38
  • 19
  • 13
  • 13
  • 8
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 7
    • 7
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-110

    Sequence

    MEGESVKLSS QTLIQAGDDE KNQRTITVNP AHMGKAFKVM NELRSKQLLC DVMIVAEDVE IEAHRVVLAA CSPYFCAMFT GDMSESKAKK IEIKDVDGQT LSKLIDYIYT

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human KLHL3 (NP_059111.2).

    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

    KLHL3 (Kelch-Like 3 (KLHL3))

    Alternative Name

    KLHL3

    Background

    This gene is ubiquitously expressed and encodes a full-length protein which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus. These kelch-like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin-RING E3 ubiquitin ligase (CRL) complex. Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D), a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.,KLHL3,PHA2D,Cell Biology & Developmental Biology,KLHL3

    Molecular Weight

    55 kDa/61 kDa/64 kDa

    Gene ID

    26249

    UniProt

    Q9UH77
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