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Anti-MMP9 (W680) Antibody |产品详情|进口橙子视频旧款采购网




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    Anti-MMP9 (W680) Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-MMP9 (W680) Antibody

    商品详情 参考文献 相关资料
    Name: Anti-MMP9 (W680) Antibody
    See all MMP9 primary antibodies
    Description: Rabbit polyclonal antibody to MMP9 (W680)
    Specificity: MMP9 (W680) pAb detects endogenous levels of MMP9 protein.
    Applications: WB, IHC, IF
    Reactivity: Human, Mouse, Rat
    Immunogen: Synthetic peptide, corresponding to amino acids 650-700 of Human MMP9.
    Host: Rabbit
    Clonality: Polyclonal
    Conjugate: Unconjugated
    Molecular Weight: ~ 92 kDa
    Purity: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
    Product Form: 1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
    Function: May play an essential role in local proteolysis of the extracellular matrix and in leukocyte migration. Could play a role in bone osteoclastic resorption. Cleaves KiSS1 at a Gly-|-Leu bond. Cleaves type IV and type V collagen into large C-terminal three quarter fragments and shorter N-terminal one quarter fragments. Degrades fibronectin but not laminin or Pz-peptide.
    Tissue Specificity: Produced by normal alveolar macrophages and granulocytes.
    Involvement in Disease: Intervertebral disc disease: A common musculo-skeletal disorder caused by degeneration of intervertebral disks of the lumbar spine. It results in low-back pain and unilateral leg pain.

    Metaphyseal anadysplasia 2: A bone development disorder characterized by skeletal anomalies that resolve spontaneously with age. Clinical characteristics are evident from the first months of life and include slight shortness of stature and a mild varus deformity of the legs. Patients attain a normal stature in adolescence and show improvement or complete resolution of varus deformity of the legs and rhizomelic micromelia.
    Sequence Similarities: Belongs to the peptidase M10A family.
    Post-Translational Modification: Processing of the precursor yields different active forms of 64, 67 and 82 kDa. Sequentially processing by MMP3 yields the 82 kDa matrix metalloproteinase-9.
    Cellular locations: Secreted > Extracellular space > Extracellular matrix.
    Database Links:
  • Entrez Gene: 4318?Human
  • Entrez Gene: 17395?Mouse
  • Entrez Gene: 81687?Rat
  • Omim: 120361?Human
  • SwissProt: P14780?Human
  • SwissProt: P41245?Mouse
  • SwissProt: P50282?Rat
  • Unigene: 297413?Human
  • Unigene: 4406?Mouse
  • Unigene: 10209?Rat
  • Synonyms:
  • 82 kDa matrix metalloproteinase-9 Antibody
  • 92 kDa gelatinase Antibody
  • 92 kDa type IV collagenase Antibody
  • CLG 4B Antibody
  • CLG4B Antibody
  • Collagenase Type 4 beta Antibody
  • Collagenase type IV 92 KD Antibody
  • EC 3.4.24.35 Antibody
  • Gelatinase 92 KD Antibody
  • Gelatinase B Antibody
  • Gelatinase beta Antibody
  • GelatinaseB Antibody
  • GELB Antibody
  • Macrophage gelatinase Antibody
  • MANDP2 Antibody
  • Matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) Antibody
  • Matrix Metalloproteinase 9 Antibody
  • MMP 9 Antibody
  • MMP-9 Antibody
  • MMP9 Antibody
  • MMP9_HUMAN Antibody
  • Type V collagenase Antibody
  • Information: Target information shown above is from the UniProt Consortium.
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