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Anti-Human TMPRSS2 Recombinant Nanobody (SAA2324) (HT176013)

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Overview
Catalog No.HT176013
Description
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Anti-Human TMPRSS2 Nanobody (SAA2324) [SAA2324] (HT176013) is a human monoclonal antibody detecting TMPRSS2 in ELISA, Inhibition. Suitable for Human.
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Species reactivityAlpaca
ApplicationsELISA, Inhibition
Host speciesHuman
IsotypeVHH-His
Clone IDSAA2324
Clonality Monoclonal
Target Transmembrane protease serine 2, EC:3.4.21.122, Serine protease 10, Transmembrane protease serine 2 non-catalytic chain, Transmembrane protease serine 2 catalytic chain, TMPRSS2, PRSS10
Endotoxin level Please contact with the lab for this information.
Purity >95% as determined by SDS-PAGE.
Purification Purified by Nickel column
Accession O15393
Form Liquid
Storage buffer 0.01M PBS pH 7.4

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Reconstitution Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Product Usage Information
Application Dilution
ELISA 1:2000-1:20000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

Transmembrane protease serine 2 (TMPRSS2) is a ~53 kDa protein. Plasma membrane-anchored serine protease that cleaves at arginine residues. Participates in proteolytic cascades of relevance for the normal physiologic function of the prostate. Androgen-induced TMPRSS2 activates several substrates that include pro-hepatocyte growth factor/HGF, the protease activated receptor-2/F2RL1 or matriptase/ST14 leading to extracellular matrix disruption and metastasis of prostate cancer cells. In addition, activates trigeminal neurons and contribute to both spontaneous pain and mechanical allodynia.

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1. Bestle, D. et al. (2020) Life science alliance 3. PMID: 32703818
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2. Fraser, BJ. et al. (2022) Nature chemical biology 18, 963-971. PMID: 35676539
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3. Wang, H. et al. (2023) Nature communications 14, 7574. PMID: 37990007
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4. McCallum, M. et al. (2024) Cell 187, 4231-4245.e13. PMID: 38964328
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5. Lucas, JM. et al. (2014) Cancer discovery 4, 1310-25. PMID: 25122198
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6. Wilson, S. et al. (2005) The Biochemical journal 388, 967-72. PMID: 15537383
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7. Ko, CJ. et al. (2015) Cancer research 75, 2949-60. PMID: 26018085
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Note For research use only
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