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KIF21A antibody (AA 1070-1270)

KIF21A Reactivity: Human WB, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7268127
  • Target See all KIF21A Antibodies
    KIF21A (Kinesin Family Member 21A (KIF21A))
    Binding Specificity
    • 2
    • 1
    • 1
    • 1
    AA 1070-1270
    Reactivity
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 6
    Rabbit
    Clonality
    • 6
    Polyclonal
    Conjugate
    • 6
    This KIF21A antibody is un-conjugated
    Application
    • 6
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Purpose
    KIF21A Rabbit pAb
    Sequence
    KQTEITSATQ NQLLFHMLKE KAELNPELDA LLGHALQDLD SVPLENVEDS TDEDAPLNSP GSEGSTLSSD LMKLCGEVKP KNKARRRTTT QMELLYADSS ELASDTSTGD ASLPGPLTPV AEGQEIGMNT ETSGTSAREK ELSPPPGLPS KIGSISRQSS LSEKKIPEPS PVTRRKAYEK AEKSKAKEQK HSDSGTSEAS L
    Cross-Reactivity
    Human, Mouse
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1070-1270 of human KIF21A (NP_001166935.1).
    Isotype
    IgG
    Top Product
    Discover our top product KIF21A Primary Antibody
  • 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
    KIF21A (Kinesin Family Member 21A (KIF21A))
    Alternative Name
    KIF21A (KIF21A Products)
    Background
    This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.,KIF21A,CFEOM1,FEOM1,FEOM3A,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,KIF21A
    Molecular Weight
    180kDa/182kDa/185kDa/187kDa
    Gene ID
    55605
    UniProt
    Q7Z4S6
    Pathways
    M Phase
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