Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to
worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting
immunostaining in relation to complex human pathologies.
TCR Screening Services
Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding.
Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".
Human (tested or 100% immunogen sequence identity)
Specificity and Use
ADAMTSL1 antibody was raised against recombinant human Punctin-1.
Recognizes the first thrombospondin repeat near the N-terminal and reacts with molecular species of 55kD or a doublet of 55kD and 60kD (glycosylated form). Note that proteolysis of Punctin-1 has been described and additional smaller bands may also be obtained.
Suitable for use in Western Blot and Immunoassays.
PBS, 0.1% BSA, 0.02% sodium azide
May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot and store at -20°C. Aliquots are stable for at least 12 months at -20°C.
ADAMTSL1 Antibody, ADAM-TS related protein 1 Antibody, ADAMTSR1 Antibody, ADAMTS-like protein 1 Antibody, ADAMTSL-1 Antibody, C9orf94 Antibody, ADAMTS-like 1 Antibody, Punctin-1 Antibody, PUNCTIN Antibody
ADAMTSL1 encodes a secreted protein and member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) family. This protein lacks the metalloproteinase and disintegrin-like domains, which are typical of the ADAMTS family, but contains other ADAMTS domains, including the thrombospondin type 1 motif. This protein may have important functions in the extracellular matrix. Alternative splicing results in multiple transcript variants encoding distinct proteins.