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MMP13 antibody (Cleaved-Tyr104)

The Rabbit Polyclonal anti-MMP13 antibody (ABIN8122795) specifically detects MMP13 in WB, IHC and ELISA. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN8122795
$225.50
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for MMP13 antibody (Cleaved-Tyr104) (ABIN8122795)

Target

See all MMP13 Antibodies
MMP13 (Matrix Metallopeptidase 13 (Collagenase 3) (MMP13))

Reactivity

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Human, Mouse, Rat

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This MMP13 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Binding Specificity

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    Cleaved-Tyr104

    Purpose

    MMP13 (Cleaved-Tyr104) Antibody

    Specificity

    This antibody detects endogenous levels of Human MMP13 (Cleaved-Tyr104, protein was cleaved amino acid sequence between 103-104 )

    Purification

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

    Immunogen

    Synthesized peptide derived from human MMP13 (Cleaved-Tyr104)

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000,IHC 1:50-300, ELISA 2000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    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/1 year

    Expiry Date

    12 months
  • Target

    MMP13 (Matrix Metallopeptidase 13 (Collagenase 3) (MMP13))

    Alternative Name

    MMP13

    Background

    Synonyms: Collagenase 3 (EC 3.4.24.-, Matrix metalloproteinase-13, MMP-13)

    Background: cofactor:Binds 2 zinc ions per subunit.,cofactor:Binds 4 calcium ions per subunit.,disease:Defects in MMP13 are the cause of spondyloepimetaphyseal dysplasia type 2 (SEMD2) [MIM:602111], also known as spondyloepimetaphyseal dysplasia type Missouri. SEMDs are a heterogeneous group of skeletal disorders characterized by defective growth and modeling of the spine and long bones. The SEMDs are distinguished from the spondylometaphyseal dysplasias and the spondyloepiphyseal dysplasias by the combined involvement of the epiphyses and metaphyses. The 3 disorders have malformations of the vertebrae in common.,domain:The conserved cysteine present in the cysteine-switch motif binds the catalytic zinc ion, thus inhibiting the enzyme. The dissociation of the cysteine from the zinc ion upon the activation-peptide release activates the enzyme.,function:Degrades collagen type I. Does not act on gelatin or casein. Could have a role in tumoral process.,similarity:Belongs to the peptidase M10A family.,similarity:Contains 4 hemopexin-like domains.,tissue specificity:Seems to be specific to breast carcinomas.,

    Gene Name: MMP13

    Protein Name: MMP13 (Cleaved-Tyr104)

    Gene ID

    4322

    UniProt

    P45452
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