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TCTN2 antibody (C-Term) (PE-Cy5)

This Rabbit Polyclonal antibody specifically detects TCTN2 in WB. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN1712965

Quick Overview for TCTN2 antibody (C-Term) (PE-Cy5) (ABIN1712965)

Target

See all TCTN2 Antibodies
TCTN2 (Tectonic Family Member 2 (TCTN2))

Reactivity

  • 24
  • 14
  • 6
  • 1
  • 1
Human, Mouse, Rat

Host

  • 28
  • 1
Rabbit

Clonality

  • 28
  • 1
Polyclonal

Conjugate

  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TCTN2 antibody is conjugated to PE-Cy5

Application

  • 27
  • 13
  • 13
  • 9
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Cross-Reactivity

    Mouse

    Predicted Reactivity

    Human,Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human TCTN2

    Isotype

    IgG
  • Application Notes

    FCM(1:100-500)
    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    TCTN2 (Tectonic Family Member 2 (TCTN2))

    Alternative Name

    TCTN2

    Background

    Synonyms: C12orf38, FLJ12975, MKS8, OTTHUMP00000239215, OTTHUMP00000239216, Tctn2, TECT2, TECT2_HUMAN, Tectonic family member 2, Tectonic-2.

    Background: Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.

    Pathways

    Proton Transport
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