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Download PDF DatasheetCatalogue No : BS1152
| Host | Reactivity | Size | Application | stock | price | cart |
| Rabbit | H,M,R | 100μg | WB IHC | ![]() |
258.00 | ![]() |
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Contact information
Email:shdiahds@163.com Click here for qusetions for this product! |
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1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
~ 28 kDa
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Granzyme B/H (E20) pAb detects endogenous levels of Granzyme B/H protein.
WB: 1:500~1:1000 IHC: 1:50~1:200

Immunohistochemistry (IHC) analyzes of Granzyme B/H (E20) pAb in paraffin-embedded human breast carcinoma tissue.
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Granzyme A and granzyme B are serine proteases that mediate apoptotic signaling in cytotoxic T lymphocytes (CTL) and natural killer (NK) cells. Both granzyme A and granzyme B are synthesized as inactive proenzymes, and they are stored within cytolytic granules and released by effector cells during degranulation. In activated CTLs, granzyme A and granzyme B are processed and activated by cathepsin C, and they then function to induce apoptosis by two distinct pathways. Granzyme B proteolytically cleaves and activates members of the caspase family of cysteine proteases, including caspase-3, caspase-6, caspase-7 and caspase-9. When cleaved, these caspases assemble into active holoenzymes that then mediate apoptosis through a defined proteolytic cascade involving nuclear lamins and PARP (poly ADP ribose polymerase). Granzyme A mediates the activation of apoptosis by inducing single-strand DNA breaks, membrane perturbation and nuclear condensations in an alternative pathway that is independent from caspase activation or the caspase proteolytic cascade.