Rabbit Polyclonal ADAMTSL2 antibody. Suitable for WB and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Recombinant Fragment Protein within Human ADAMTSL2 aa 750-950.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
WB | |
---|---|
Human | Tested |
Mouse | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500.00000 - 1/3000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
KIAA0605, ADAMTSL2, ADAMTS-like protein 2, ADAMTSL-2
Rabbit Polyclonal ADAMTSL2 antibody. Suitable for WB and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Recombinant Fragment Protein within Human ADAMTSL2 aa 750-950.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
ADAMTSL2 also known as ADAMTS-like 2 is a secreted glycoprotein that belongs to the family of ADAMTS-like proteins. The molecular mass of this protein is approximately 65 kDa. ADAMTSL2 expresses predominantly in connective tissues and various organs including the skin cartilage and lung tissues. It shares structural similarities with other members of the ADAMTS family but lacks the protease domain which is essential for proteolytic activity in related proteins.
ADAMTSL2 plays an important role in extracellular matrix organization and assembly. It is not part of a known complex but it interacts closely with fibrillin-1 influencing the regulation of microfibril architecture. The presence of ADAMTSL2 can impact the deposition and maintenance of elastic fibers contributing significantly to the structural integrity of connective tissues.
The presence of ADAMTSL2 is integral to the TGF-beta signaling pathway and extracellular matrix-receptor interaction pathway. It modulates the bioavailability of latent TGF-beta by interacting with fibrillin-1 and indirectly influencing the activity of proteins like LTBP4. These interactions play a role in maintaining proper tissue architecture and cellular functions by mediating signaling cascades essential for tissue repair and homeostasis.
Mutations in the ADAMTSL2 gene associate with geleophysic dysplasia a rare skeletal disorder characterized by short stature and heart valve abnormalities. The connection to fibrillin-1 further links ADAMTSL2 to disorders such as Marfan syndrome though through indirect pathways rather than direct genetic links. The involvement of other proteins in this process such as LTBP4 and fibrillin-1 helps elucidate the molecular mechanisms underlying these conditions.
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7.5% SDS PAGE
All lanes: Western blot - Anti-ADAMTSL2 antibody (ab97603) at 1/500 dilution
All lanes: H1299 whole cell lysate at 30 µg
Predicted band size: 104 kDa
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