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MKKS antibody

MKKS Reactivity: Human, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7074572
  • Target See all MKKS Antibodies
    MKKS (McKusick-Kaufman Syndrome (MKKS))
    Reactivity
    • 38
    • 1
    • 1
    Human, Rat
    Host
    • 37
    • 1
    Rabbit
    Clonality
    • 38
    Polyclonal
    Conjugate
    • 14
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MKKS antibody is un-conjugated
    Application
    • 37
    • 18
    • 13
    • 13
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Cross-Reactivity
    Human, Rat
    Purification
    Affinity purification
    Immunogen
    Recombinant protein corresponding to Mouse MKKS
    Top Product
    Discover our top product MKKS Primary Antibody
  • Application Notes
    WB (H,R) 1:1000-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • Target
    MKKS (McKusick-Kaufman Syndrome (MKKS))
    Alternative Name
    MKKS (MKKS Products)
    Synonyms
    bbs6 antibody, zgc:55608 antibody, MKKS antibody, kms antibody, mks antibody, hmcs antibody, DKFZp459L0833 antibody, BBS6 antibody, HMCS antibody, KMS antibody, MKS antibody, 1300013E18Rik antibody, AI463362 antibody, AI957237 antibody, Bbs6 antibody, McKusick-Kaufman syndrome antibody, Mkks antibody, mkks antibody, MKKS antibody
    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.
    Molecular Weight
    62 kDa
    Gene ID
    59030
    NCBI Accession
    NP_001135418
    UniProt
    Q9JI70
    Pathways
    Sensory Perception of Sound
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