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ANKRD15 antibody (AA 900-1000)

This anti-ANKRD15 antibody is a Rabbit Polyclonal antibody detecting ANKRD15 in WB and IF. Suitable for Human.
Catalog No. ABIN7265613

Quick Overview for ANKRD15 antibody (AA 900-1000) (ABIN7265613)

Target

See all ANKRD15 Antibodies
ANKRD15 (Ankyrin Repeat Domain 15 (ANKRD15))

Reactivity

  • 13
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 10
  • 3
Rabbit

Clonality

  • 10
  • 3
Polyclonal

Conjugate

  • 10
  • 1
  • 1
  • 1
This ANKRD15 antibody is un-conjugated

Application

  • 9
  • 6
  • 3
  • 2
  • 2
  • 2
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 900-1000

    Purpose

    KANK1 Rabbit pAb

    Sequence

    GNYLGYTCKC GGLQSGSPLS SQTSQPEQEV GTSEGKPISS LDAFPTQEGT LSPVNLTDDQ IAAGLYACTN NESTLKSIMK KKDGNKDSNG AKKNLQFVGI N

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic peptide corresponding to a sequence within amino acids 900-1000 of human KANK1 (NP_055973.2).

    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

    ANKRD15 (Ankyrin Repeat Domain 15 (ANKRD15))

    Alternative Name

    KANK1

    Background

    The protein encoded by this gene belongs to the Kank family of proteins, which contain multiple ankyrin repeat domains. This family member functions in cytoskeleton formation by regulating actin polymerization. This gene is a candidate tumor suppressor for renal cell carcinoma. Mutations in this gene cause cerebral palsy spastic quadriplegic type 2, a central nervous system development disorder. A t(5,9) translocation results in fusion of the platelet-derived growth factor receptor beta gene (PDGFRB) on chromosome 5 with this gene in a myeloproliferative neoplasm featuring severe thrombocythemia. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 20.,KANK1,ANKRD15,CPSQ2,KANK,Cancer,Tumor suppressors,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Microfilaments,KANK1

    Molecular Weight

    129kDa/147kDa

    Gene ID

    23189

    UniProt

    Q14678

    Pathways

    Regulation of Actin Filament Polymerization
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