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MMP26 antibody (AA 96-125)

The Rabbit Polyclonal anti-MMP26 antibody has been validated for WB. It is suitable to detect MMP26 in samples from Human.
Catalog No. ABIN5537136

Quick Overview for MMP26 antibody (AA 96-125) (ABIN5537136)

Target

See all MMP26 Antibodies
MMP26 (Matrix Metallopeptidase 26 (MMP26))

Reactivity

  • 40
  • 2
  • 2
  • 1
Human

Host

  • 34
  • 6
Rabbit

Clonality

  • 34
  • 6
Polyclonal

Conjugate

  • 15
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MMP26 antibody is un-conjugated

Application

  • 34
  • 14
  • 13
  • 13
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 7
    • 3
    • 3
    • 2
    • 1
    • 1
    AA 96-125

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This MMP26 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 96-125 amino acids from the Central region of human MMP26.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    MMP26 (Matrix Metallopeptidase 26 (MMP26))

    Alternative Name

    MMP26

    Background

    Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The encoded protein degrades type IV collagen, fibronectin, fibrinogen, casein, vitronectin, alpha 1-antitrypsin, alpha 2-macroglobulin, and insulin-like growth factor-binding protein 1, and activates MMP9 by cleavage. The protein differs from most MMP family members in that it lacks a conserved C-terminal protein domain.

    Molecular Weight

    30 kDa

    Gene ID

    56547

    UniProt

    Q9NRE1
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