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KIF21A antibody (AA 1070-1270)

This anti-KIF21A antibody is a Rabbit Polyclonal antibody detecting KIF21A in WB and IF. Suitable for Human.
Catalog No. ABIN7268127

Quick Overview for KIF21A antibody (AA 1070-1270) (ABIN7268127)

Target

See all KIF21A Antibodies
KIF21A (Kinesin Family Member 21A (KIF21A))

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)
  • Binding Specificity

    • 2
    • 1
    • 1
    • 1
    AA 1070-1270

    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
  • 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

    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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