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CEP57L1 antibody (AA 131-230) (Cy5.5)

This Rabbit Polyclonal antibody specifically detects CEP57L1 in WB, IF (cc), IF (p). It exhibits reactivity toward Human.
Catalog No. ABIN1706683

Quick Overview for CEP57L1 antibody (AA 131-230) (Cy5.5) (ABIN1706683)

Target

See all CEP57L1 Antibodies
CEP57L1 (Centrosomal Protein 57kDa-Like 1 (CEP57L1))

Reactivity

  • 20
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 20
Rabbit

Clonality

  • 20
Polyclonal

Conjugate

  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CEP57L1 antibody is conjugated to Cy5.5

Application

  • 20
  • 12
  • 12
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

    • 14
    • 2
    • 1
    • 1
    • 1
    AA 131-230

    Predicted Reactivity

    Human,Mouse,Rat,Dog,Sheep,Pig,Rabbit

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C6ORF182

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    CEP57L1 (Centrosomal Protein 57kDa-Like 1 (CEP57L1))

    Alternative Name

    C6orf182

    Background

    Synonyms: BA487F23.2, Centrosomal protein of 57 kDa-related protein, Cep57-related protein, CEP57R, Chromosome 6 open reading frame 182, Hypothetical protein LOC285753, MGC21731, MGC70837, OTTHUMP00000016948,CE57L_HUMAN.

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf182 gene product has been provisionally designated C6orf182 pending further characterization.

    Gene ID

    285753

    Pathways

    Maintenance of Protein Location
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