ADAMTS-1 Rabbit Polyclonal Antibody |
|||
| ES1599-100ul | ELK Biotech | 100ul | 124 EUR |
|
Description: WB, ELISA |
|||
ADAMTS-1 Rabbit Polyclonal Antibody |
|||
| ES1599-50ul | ELK Biotech | 50ul | 74 EUR |
|
Description: WB, ELISA |
|||
ADAMTS-12 Rabbit Polyclonal Antibody |
|||
| ES7651-100ul | ELK Biotech | 100ul | 124 EUR |
|
Description: IHC, ELISA |
|||
ADAMTS-12 Rabbit Polyclonal Antibody |
|||
| ES7651-50ul | ELK Biotech | 50ul | 74 EUR |
|
Description: IHC, ELISA |
|||
ADAMTS-18 Rabbit Polyclonal Antibody |
|||
| ES8418-100ul | ELK Biotech | 100ul | 124 EUR |
|
Description: WB, IHC, ELISA |
|||
ADAMTS-18 Rabbit Polyclonal Antibody |
|||
| ES8418-50ul | ELK Biotech | 50ul | 74 EUR |
|
Description: WB, IHC, ELISA |
|||
ADAMTS-16 Rabbit Polyclonal Antibody |
|||
| ES5000-100ul | ELK Biotech | 100ul | 124 EUR |
|
Description: IHC, ELISA |
|||
ADAMTS-16 Rabbit Polyclonal Antibody |
|||
| ES5000-50ul | ELK Biotech | 50ul | 74 EUR |
|
Description: IHC, ELISA |
|||
ADAMTS-17 Rabbit Polyclonal Antibody |
|||
| ES5001-100ul | ELK Biotech | 100ul | 124 EUR |
|
Description: IHC, ELISA |
|||
ADAMTS-17 Rabbit Polyclonal Antibody |
|||
| ES5001-50ul | ELK Biotech | 50ul | 74 EUR |
|
Description: IHC, ELISA |
|||
ADAMTS-19 Rabbit Polyclonal Antibody |
|||
| ES5003-100ul | ELK Biotech | 100ul | 124 EUR |
|
Description: WB, ELISA |
|||
ADAMTS-19 Rabbit Polyclonal Antibody |
|||
| ES5003-50ul | ELK Biotech | 50ul | 74 EUR |
|
Description: WB, ELISA |
|||
Rabbit polyclonal antibody to ADAMTSL2 (ADAMTS-like 2) |
|||
| TA308981 | Origene Technologies GmbH | 100 µl | Ask for price |
Rabbit anti-human ADAMTS-like 4 polyclonal Antibody |
|||
| MBS716409-01mL | MyBiosource | 0.1mL | 485 EUR |
Rabbit anti-human ADAMTS-like 4 polyclonal Antibody |
|||
| MBS716409-5x01mL | MyBiosource | 5x0.1mL | 2175 EUR |
ADAMTS-2 Polyclonal Antibody |
|||
| ABP57362-003ml | Abbkine | 0.03ml | 189.6 EUR |
|
Description: A polyclonal antibody for detection of ADAMTS-2 from Human. This ADAMTS-2 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ADAMTS-2 at AA range: 1140-1220 |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| ABP57362-01ml | Abbkine | 0.1ml | 346.8 EUR |
|
Description: A polyclonal antibody for detection of ADAMTS-2 from Human. This ADAMTS-2 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ADAMTS-2 at AA range: 1140-1220 |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| ABP57362-02ml | Abbkine | 0.2ml | 496.8 EUR |
|
Description: A polyclonal antibody for detection of ADAMTS-2 from Human. This ADAMTS-2 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ADAMTS-2 at AA range: 1140-1220 |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| BT-AP00249-100ul | Jiaxing Korain Biotech Ltd (BT Labs) | 100ul | Ask for price |
|
Description: ADAMTS2 (ADAM metallopeptidase with thrombospondin type 1 motif 2) encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| BT-AP00249-20ul | Jiaxing Korain Biotech Ltd (BT Labs) | 20ul | Ask for price |
|
Description: ADAMTS2 (ADAM metallopeptidase with thrombospondin type 1 motif 2) encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| BT-AP00249-50ul | Jiaxing Korain Biotech Ltd (BT Labs) | 50ul | Ask for price |
|
Description: ADAMTS2 (ADAM metallopeptidase with thrombospondin type 1 motif 2) encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| JOT-AP00249-100ul | Jotbody | 100ul | 220 EUR |
|
Description: Human |
|||
ADAMTS-2 Polyclonal Antibody |
|||
| JOT-AP00249-50ul | Jotbody | 50ul | 144 EUR |
|
Description: Human |
|||