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MKRN3 antibody (AA 1-260)

The Rabbit Polyclonal anti-MKRN3 antibody has been validated for WB. It is suitable to detect MKRN3 in samples from Human.
Catalog No. ABIN7268378

Quick Overview for MKRN3 antibody (AA 1-260) (ABIN7268378)

Target

MKRN3 (Makorin Ring Finger Protein 3 (MKRN3))

Reactivity

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

Host

  • 12
  • 2
Rabbit

Clonality

  • 12
  • 2
Polyclonal

Conjugate

  • 9
  • 1
  • 1
  • 1
  • 1
  • 1
This MKRN3 antibody is un-conjugated

Application

  • 12
  • 12
  • 4
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-260

    Purpose

    MKRN3 Rabbit pAb

    Sequence

    MEEPAAPSEA HEAAGAQAGA EAAREGVSGP DLPVCEPSGE SAAPDSALPH AARGWAPFPV APVPAHLRRG GLRPAPASGG GAWPSPLPSR SSGIWTKQII CRYYIHGQCK EGENCRYSHD LSGRKMATEG GVSPPGASAG GGPSTAAHIE PPTQEVAEAP PAASSLSLPV IGSAAERGFF EAERDNADRG AAGGAGVESW ADAIEFVPGQ PYRGRWVASA PEAPLQSSET ERKQMAVGSG LRFCYYASRG VCFRGESCMY

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human MKRN3 (NP_005655.1).

    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

    MKRN3 (Makorin Ring Finger Protein 3 (MKRN3))

    Alternative Name

    MKRN3

    Background

    The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene.,MKRN3,CPPB2,D15S9,RNF63,ZFP127,ZNF127,MKRN3

    Molecular Weight

    55kDa

    Gene ID

    7681

    UniProt

    Q13064
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