BBS6 antibody

Cat.#: 108373

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Product Information

  • Product Name
    BBS6 antibody
  • Documents
  • Description
    BBS6 Rabbit Polyclonal antibody. Positive IF detected in hTERT-RPE1 cells. Positive WB detected in mouse testis tissue, mouse brain tissue. Observed molecular weight by Western-blot: 63kd
  • Tested applications
    ELISA, WB, IF
  • Species reactivity
    Human,Mouse,Rat; other species not tested.
  • Alternative names
    BBS6 antibody; HMCS antibody; KMS antibody; McKusick Kaufman syndrome antibody; MKKS antibody; MKS antibody
  • Isotype
    Rabbit IgG
  • Preparation
    This antibody was obtained by immunization of BBS6 recombinant protein (Accession Number: NM_018848). Purification method: Antigen affinity purified.
  • Clonality
    Polyclonal
  • Formulation
    PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
  • Storage instructions
    Store at -20℃. DO NOT ALIQUOT
  • Applications

    Recommended Dilution:

    WB: 1:200-1:1000

    IF: 1:20-1:200

  • Validations

    IF result (cytoplasm and the base of cilia stain) of anti-BBS6 (Catalog No:108373; 1:50) with hTERT-RPE1 cell (MeOH fixed) by Dr. Moshe Kim.

    IF result (cytoplasm and the base of cilia stain) of anti-BBS6 (Catalog No:108373; 1:50) with hTERT-RPE1 cell (MeOH fixed) by Dr. Moshe Kim.

    mouse testis tissue were subjected to SDS PAGE followed by western blot with Catalog No:108373(BBS6 antibody) at dilution of 1:600

    mouse testis tissue were subjected to SDS PAGE followed by western blot with Catalog No:108373(BBS6 antibody) at dilution of 1:600

  • Background
    MKKS also known as BBS6 is a probable chaperone given to the amino acid similarity to the chaperonin family of proteins and may play a role in protein processing in limb, cardiac and reproductive system development. The mutations in BBS6 have been linked to Bardet-Biedl syndrome (BBS) which is a genetically heterogeneous, autosomal recessive disorder characterized by usually severe pigmentary retinopathy, early onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. It may also get involved in cellular organization processes, in particular relating to ciliary/flagellar and centrosomal activities.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"