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> Antibody > Rabbit PAb Antibody > KLK-7 / Kallikrein-7 / PRSS6 Antibody (Antigen Affinity Purified) KLK-7 / Kallikrein-7 / PRSS6 Antibody (Antigen Affinity Purified)
| Catalog | Size (Price) | Quantity | In Stock | Operation | Other Information |
| 10416-RP02 |
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YES |
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Kallikrein-7 / PRSS6 / KLK7 Antibody ( Antigen Affinity Purified )
| Order or Inquire for KLK7 Antibody product | ![]() |
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| Detection limit is 0.5 ng/lane in WB | |||
| Detection limit is 0.00245 ng/well in ELISA |
Kallikrein-7 / PRSS6 / KLK7 Antibody Product Information
| Immunogen : |
Recombinant human KLK7 protein ( Catalog#10416-H08H ) |
| Antibody Type : | Rabbit Polyclonal Antibody ( Antibody Purification Platform ) |
| Ig Type : |
Rabbit IgG |
| Formulation : | 0.2 μm filtered solution in PBS with 5% trehalose |
| Preparation : |
Produced in rabbits immunized with purified, human cell-derived, recombinant human KLK7 ( rh KLK7 ; Catalog#10416-H08H ; NP_005037.1 ; Met 1 - Arg 253 ). KLK7 specific IgG was purified by human KLK7 affinity chromatography |
Kallikrein-7 / PRSS6 / KLK7 Antibody Usage Guide
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Specificity : |
Human Kallikrein-7 / KLK7 |
| Western blot : | This antibody can be used at 0.1 - 0.2 μg/mL with the appropriate secondary reagents to detect human KLK7 in WB. Using a DAB detection system, the detection limit for human KLK7 is approximately 0.5 ng/lane under non-reducing conditions and 1 ng/lane under reducing conditions |
| Direct ELISA : | This antibody can be used at 0.1 - 0.2 μg/mL with the appropriate secondary reagents to detect human KLK7. The detection limit for human KLK7 is approximately 0.00245 ng/well |
| Storage : | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free. Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles. |
Kallikrein-7 / PRSS6 / KLK7 Antibody Related Products & Topics
Related Areas:
Enzyme>>Protease & Regulator>>Serine Protease & Regulator>>Kallikrein>>KLK7/Kallikrein 7
Cancer>>Angiogenesis>>Kallikrein>>KLK7/Kallikrein 7
Proteins:
| Molecule | Species | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| KLK7/Kallikrein 7 | Human | KLK7/Kallikrein 7 Protein, Recombinant![]() |
10416-H08H |
Antibodies:
| Molecule | Application | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| Human KLK7/Kallikrein 7 |
WB, ELISA | KLK7/Kallikrein 7 Antibody, Rabbit PAb | 10416-RP01 |
| Human KLK7/Kallikrein 7 |
WB, ELISA | KLK7/Kallikrein 7 Antibody, Rabbit PAb (Antigen Affinity Purified) | 10416-RP02 |
Kallikrein-7 / PRSS6 / KLK7 Antibody Background
Kallikrein-7, also known as kallikrein-related peptidase 7, Stratum corneum chymotryptic enzyme, Serine protease 6, KLK7, and PRSS6, is a secreted protein which belongs to the peptidase S1 family and Kallikrein subfamily. Members of the Kallikrein family are involved in various malignancies such as prostate ( PSA, KLK2, KLK15 ), ovarian ( KLK4, KLK5, KLK6, KLK8, KLK10 ), and breast cancer ( KLK10, KLK13, KLK14 ). Kallikrein-7 / KLK7 appears to be increased in ovarian cancer and higher KLK7 expression in ovarian cancer tissue is associated with poorer prognosis of ovarian cancer patients. Kallikrein-7 / KLK7 is abundantly expressed in the skin and is expressed by keratinocytes in the epidermis. Kallikrein-7 / KLK7 is up-regulated in ovarian carcinoma, especially late-stage serous carcinoma, compared with normal ovaries and benign adenomas (at the protein level). It was significantly associated with shorter overall survival (OS) and disease-free survival (DFS). Kallikrein-7 / KLK7 may catalyze the degradation of intercellular cohesive structures in the cornified layer of the skin in the continuous shedding of cells from the skin surface. KLK7 also plays a role in the activation of precursors to inflammatory cytokines
References
- Dong,Y. et al., 2003, Clin Cancer Res. 9 (5):1710-20.
- Kyriakopoulou, LG. et al., 2003, Clin Biochem. 36 (2):135-43.
- Talieri, M. et al.,2004,Thromb Haemost. 91 (1):180-6.
- Talieri, M. et al., 2009, Thromb Haemost. 101 (4): 741-7.
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