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Anti-C2orf61 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Anti-C2orf61 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Catalog # 76098-250
Supplier:  Bioss
Anti-C2orf61 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Catalog # 76098-250
Supplier:  Bioss
Supplier Number:  BS-15155R-A680

Specifications

  • Antibody Type:
    Primary
  • Antigen Name:
    C2orf61
  • Clonality:
    Polyclonal
  • Conjugation:
    Alexa Fluor® 680
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Western Blot:
    Yes
  • Size:
    100 µl
  • Epitope:
    21-120/248
  • Form:
    Liquid
  • Gene ID:
    285051
  • Antigen Synonyms:
    CB061_HUMAN|DKFZp434N1418|Uncharacterized protein C2orf61|CCDC113|HSPC065|Chromosome 2 open reading frame 61|Coiled-coil domain-containing protein 113 Gene names
  • Modification:
    Unmodified
  • Storage Buffer:
    Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
  • Molecular Weight:
    19 kDa
  • Storage Temperature:
    Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Concentration:
    1 µg/µl
  • Shipping Temperature:
    4 °C
  • Immunogen:
    KLH conjugated synthetic peptide derived from human C2orf61
  • Tested Applications:
    ICC
  • Purification:
    Purified by Protein A
  • Cat. No.:
    76098-250
  • Packaging:
    Vial

Specifications

About this item

C2orf61 (chromosome 2 open reading frame 61), also known as FLJ40172, is a 177 amino acid protein encoded by a gene that maps to human chromosome 2p21. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Type: Primary
Antigen: C2orf61
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 680
Public Immunogen Range: 21-120/248
Host: Rabbit
Isotype: IgG
Reactivity: