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POGLUT1 antibody (AA 160-280)

This Rabbit Polyclonal antibody specifically detects POGLUT1 in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7269673

Quick Overview for POGLUT1 antibody (AA 160-280) (ABIN7269673)

Target

See all POGLUT1 Antibodies
POGLUT1 (Protein O-Glucosyltransferase 1 (POGLUT1))

Reactivity

  • 19
  • 17
  • 2
  • 1
  • 1
Human

Host

  • 33
  • 1
Rabbit

Clonality

  • 33
  • 1
Polyclonal

Conjugate

  • 12
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This POGLUT1 antibody is un-conjugated

Application

  • 30
  • 15
  • 13
  • 13
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 15
    • 8
    • 5
    • 4
    • 2
    • 1
    • 1
    AA 160-280

    Purpose

    POGLUT1 Rabbit pAb

    Sequence

    MYPAWTFWEG GPAVWPIYPT GLGRWDLFRE DLVRSAAQWP WKKKNSTAYF RGSRTSPERD PLILLSRKNP KLVDAEYTKN QAWKSMKDTL GKPAAKDVHL VDHCKYKYLF NFRGVAASFR F

    Cross-Reactivity

    Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 160-280 of human POGLUT1 (NP_689518.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,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

    POGLUT1 (Protein O-Glucosyltransferase 1 (POGLUT1))

    Alternative Name

    POGLUT1

    Background

    This gene encodes a protein with both O-glucosyltransferase and O-xylosyltransferase activity which localizes to the lumen of the endoplasmic reticulum. This protein has a carboxy-terminal KTEL motif which is predicted to function as an endoplasmic reticulum retention signal. This gene is an essential regulator of Notch signalling and likely plays a role in cell fate and tissue formation during development. It may also play a role in the pathogenesis of leukemia. Mutations in this gene have been associated with the autosomal dominant genodermatosis Dowling-Degos disease 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014],C3orf9,CLP46,KDELCL1,KTELC1,LGMD2Z,MDS010,MDSRP,Rumi,hCLP46,POGLUT1,Cell Biology & Developmental Biology,POGLUT1

    Gene ID

    56983

    UniProt

    Q8NBL1

    Pathways

    Notch Signaling
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