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Granzyme K Recombinant Rabbit Monoclonal Antibody [PSH16-28]

Usd: 385

Specification

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Catalog# HA723826

Granzyme K Recombinant Rabbit Monoclonal Antibody [PSH16-28]

Application

  • WB

  • IHC-P

  • IF-Tissue

Reactivity

  • Human

BSA and Azide free
Conjugation

  • unconjugated

Overview

Product Name

Granzyme K Recombinant Rabbit Monoclonal Antibody [PSH16-28]

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human Granzyme K aa 1-264.

Species Reactivity

Human

Validated Applications

WB, IHC-P, IF-Tissue

Molecular Weight

Predicted band size: 29 kDa

Positive Control

NK-92 cell lysate, human NK/T lymphoma tissue.

Conjugation

unconjugated

Clone Number

PSH16-28

Reactivity Data

WB IHC-P IF-Tissue
Human
Tested Tested
Tested Tested
Mouse
Not Recommended
Not Recommended
Rat
Not Recommended
Not Recommended

Product Features

Form

Liquid

Concentration

Storage Instructions

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.

Storage Buffer

1*PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.2% Proclean 950.

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

  • WB

  • 1:5,000

  • IHC-P

  • 1:1,000

  • IF-Tissue

  • 1:500

Target

Function

Granzyme K (GzmK) is a serine protease that sits in the dense-core granules of cytotoxic T lymphocytes and NK cells. While its gene neighbors encode granzymes A–C, GzmK stands out by lacking the N-linked glycosylation motifs that decorate most family members; this minimalist design keeps it stable at the low pH of the granule and allows it to emerge in an immediately active form once perforin has punched entry holes in a target cell. Inside the cytosol, GzmK bypasses the canonical caspase cascade: it clips Bid to tBid, nicks the anti-apoptotic SET complex, and generates single-stranded DNA nicks that push the cell into a swift form of death intermediate between apoptosis and necrosis. In addition, any GzmK that leaks into the extracellular space can process pro-IL-1β and activate PAR-2 on macrophages and endothelial cells, turning a private hit into a broader inflammatory alert.

Background References

1. Jonsson AH et al. Granzyme K+ CD8 T cells form a core population in inflamed human tissue. Sci Transl Med. 2022 Jun

2. Guo CL et al. Granzyme K+CD8+ T cells interact with fibroblasts to promote neutrophilic inflammation in nasal polyps. Nat Commun. 2024 Nov

Subcellular Location

Secreted, Cytoplasmic granule.

UNIPROT

SwissProt: P49863 Human

Synonyms

Fragmentin 3 antibody

Fragmentin-3 antibody

Fragmentin3 antibody

GRAK_HUMAN antibody

Granzyme 3 antibody

granzyme K (granzyme 3

tryptase II) antibody

granzyme K (serine protease, granzyme 3

tryptase II) antibody

Granzyme K antibody

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Western blot analysis of Granzyme K on different lysates with Rabbit anti-Granzyme K antibody (<a href="/products/HA723826" style="font-weight: bold;text-decoration: underline;">HA723826</a>) at 1/5,000 dilution.<br /><br />Lane 1: NK-92 cell lysate (20 µg/Lane)<br />Lane 2: HeLa cell lysate (negative) (20 µg/Lane)<br /><br />Predicted band size: 29 kDa<br />Observed band size: 27 kDa<br /><br />Exposure time: 10 seconds; ECL: K1801;<br /><br />4-20% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA723826" style="font-weight: bold;text-decoration: underline;">HA723826</a>) at 1/5,000 dilution was used in primary antibody dilution (<a href="/products/K1803" style="font-weight: bold;text-decoration: underline;">K1803</a>) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1/50,000 dilution was used for 1 hour at room temperature.

    ☑ Relative expression (RE)

    Western blot analysis of Granzyme K on different lysates with Rabbit anti-Granzyme K antibody (HA723826) at 1/5,000 dilution.

    Lane 1: NK-92 cell lysate (20 µg/Lane)
    Lane 2: HeLa cell lysate (negative) (20 µg/Lane)

    Predicted band size: 29 kDa
    Observed band size: 27 kDa

    Exposure time: 10 seconds; ECL: K1801;

    4-20% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723826) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

  • Immunohistochemical analysis of paraffin-embedded human NK/T lymphoma tissue with Rabbit anti-Granzyme K antibody (<a href="/products/HA723826" style="font-weight: bold;text-decoration: underline;">HA723826</a>) at 1/1,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA723826" style="font-weight: bold;text-decoration: underline;">HA723826</a>) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded human NK/T lymphoma tissue with Rabbit anti-Granzyme K antibody (HA723826) at 1/1,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA723826) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Immunohistochemical analysis of paraffin-embedded human pancreas tissue (negative) with Rabbit anti-Granzyme K antibody (<a href="/products/HA723826" style="font-weight: bold;text-decoration: underline;">HA723826</a>) at 1/200 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA723826" style="font-weight: bold;text-decoration: underline;">HA723826</a>) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    ☑ Relative expression (RE)

    Immunohistochemical analysis of paraffin-embedded human pancreas tissue (negative) with Rabbit anti-Granzyme K antibody (HA723826) at 1/200 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA723826) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Application: IF-Tissue<br /><br />Species: Human<br /><br />Site: NK/T lymphoma<br /><br />Sample: Paraffin-embedded section<br /><br />Antibody concentration: 1/500

    Application: IF-Tissue

    Species: Human

    Site: NK/T lymphoma

    Sample: Paraffin-embedded section

    Antibody concentration: 1/500

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"