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antibody from antibodies-online
Targeting: ADAMTS13
C9orf8, DKFZp434C2322, FLJ42993, MGC118899, MGC118900, TTP, vWF-CP, VWFCP
Western blotAntibody data
- Antibody Data
- Antigen structure
- References [7]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
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- Product number
- ABIN359601 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 836-866) antibody
- Antibody type
- Polyclonal
- Description
- Protein A Chromatography, followed by peptide affinity purification.
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 836-866
- Vial size
- 0.4 mL
- Storage
- Store the antibody undiluted at 2-8°C for one month or (in aliquots) at-20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Zinc and calcium ions cooperatively modulate ADAMTS13 activity.
Modulation of ADAMTS13 secretion and specific activity by a combination of common amino acid polymorphisms and a missense mutation.
Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13.
Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.
Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains.
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura.
Anderson PJ, Kokame K, Sadler JE
The Journal of biological chemistry 2006 Jan 13;281(2):850-7
The Journal of biological chemistry 2006 Jan 13;281(2):850-7
Modulation of ADAMTS13 secretion and specific activity by a combination of common amino acid polymorphisms and a missense mutation.
Plaimauer B, Fuhrmann J, Mohr G, Wernhart W, Bruno K, Ferrari S, Konetschny C, Antoine G, Rieger M, Scheiflinger F
Blood 2006 Jan 1;107(1):118-25
Blood 2006 Jan 1;107(1):118-25
Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13.
Pimanda JE, Maekawa A, Wind T, Paxton J, Chesterman CN, Hogg PJ
Blood 2004 Jan 15;103(2):627-9
Blood 2004 Jan 15;103(2):627-9
Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.
Zheng X, Nishio K, Majerus EM, Sadler JE
The Journal of biological chemistry 2003 Aug 8;278(32):30136-41
The Journal of biological chemistry 2003 Aug 8;278(32):30136-41
Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains.
Cal S, Obaya AJ, Llamazares M, Garabaya C, Quesada V, López-Otín C
Gene 2002 Jan 23;283(1-2):49-62
Gene 2002 Jan 23;283(1-2):49-62
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM
Nature 2001 Oct 4;413(6855):488-94
Nature 2001 Oct 4;413(6855):488-94
Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura.
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K
The Journal of biological chemistry 2001 Nov 2;276(44):41059-63
The Journal of biological chemistry 2001 Nov 2;276(44):41059-63
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Supportive validation
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- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC
