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FERMT1 antibody (AA 216-677)

The Mouse Monoclonal anti-FERMT1 antibody is suitable to detect FERMT1 in samples from Human. It has been validated for WB and IHC (p).
Catalog No. ABIN7872243
$640.46
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for FERMT1 antibody (AA 216-677) (ABIN7872243)

Target

See all FERMT1 Antibodies
FERMT1 (Fermitin Family Member 1 (FERMT1))

Reactivity

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Human

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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This FERMT1 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Grade

Carrier-free

Clone

4A5-14
  • Binding Specificity

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    AA 216-677

    Purpose

    Kindlin-1 Antibody / KIND1 (azide and preservative free)

    Purification

    Protein G affinity chromatography

    Immunogen

    Amino acids 216-677 from the human protein were used as the immunogen for the Kindlin-1 antibody.

    Isotype

    IgG2a
  • Application Notes

    Optimal dilution of the Kindlin-1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    4 °C,-20 °C

    Storage Comment

    Store the Kindlin-1 antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • Target

    FERMT1 (Fermitin Family Member 1 (FERMT1))

    Alternative Name

    Kindlin-1

    Background

    Kindlin-1 (also known as KIND1, KINDLERIN, UNC112-RELATED PROTEIN 1 (URP1) is an important component of cell-extracellular matrix adhesion. Kindlin-1 is involved in cell adhesion, possibly via its interaction with integrins and may mediate TGF-beta 1 signaling during tumor progression. Kindlin-1 has been shown to be significantly upregulated in lung and colon carcinomas. Mutations in the kindlin-1 gene, FERMT1, causes Kindler syndrome. Kindler syndrome is an autosomal recessive disorder characterized by neonatal blistering, sun sensitivity, atrophy, abnormal pigmentation and fragility of the skin. We have developed monoclonal anti-kidlin-1 antibodies. This monoclonal antibody recognizes kindlin-1 in multiple assays including Western blotting, immunoprecipitation, immunohistochemical and immunofluorescent staining.

    UniProt

    Q9BQL6
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