HPSE Polyclonal antibody

HPSE Polyclonal Antibody for IF, IHC, WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse and More (1)

Applications

WB, IHC, IF, ELISA

Conjugate

Unconjugated

Cat no : 24529-1-AP

Synonyms

Endo glucoronidase, HEP, heparanase, Heparanase 1, HPA, Hpa1, HPR1, HPSE, HPSE1, HSE1



Tested Applications

Positive WB detected inHeLa cells, HepG2 cells, Jurkat cells, mouse liver tissue
Positive IHC detected inhuman liver cancer tissue, human placenta tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF detected inHeLa cells, HepG2 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:1000-1:8000
Immunohistochemistry (IHC)IHC : 1:20-1:200
Immunofluorescence (IF)IF : 1:10-1:100
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

24529-1-AP targets HPSE in WB, IHC, IF, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Cited Reactivityhuman, mouse, rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen HPSE fusion protein Ag21479
Full Name heparanase
Calculated Molecular Weight 543 aa, 61 kDa
Observed Molecular Weight 60 kDa
GenBank Accession NumberBC051321
Gene Symbol HPSE
Gene ID (NCBI) 10855
RRIDAB_2879591
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

HPSE(Heparanase) is also named as HEP, HPA, HPA1, HPR1, HPSE1, HSE1 and belongs to the glycosyl hydrolase 79 family. It is a endoglycosidase that cleaves heparan sulfate proteoglycans (HSPGs) into heparan sulfate side chains and core proteoglycans. HPSE is essential in the disassembly of the extracellular matrix (ECM) by invading cells. It has 3 isoforms produced by alternative splicing with the molecular weight of 61 kDa, 55 kDa and 53 kDa. The full length protein has six glycosylation sites. The cleavage of the 65 kDa form leads to the generation of a linker peptide, and 8 kDa and 50 kDa products. The active form, the 8/50 kDa heterodimer, is resistant to degradation and glycosylation of the 50 kDa subunit appears to be essential for its solubility.

Protocols

Product Specific Protocols
WB protocol for HPSE antibody 24529-1-APDownload protocol
IHC protocol for HPSE antibody 24529-1-APDownload protocol
IF protocol for HPSE antibody 24529-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

J Control Release

cRGD-targeted heparin nanoparticles for effective dual drug treatment of cisplatin-resistant ovarian cancer

Authors - Xiaomei Liang
humanWB,IHC

EMBO Rep

CircHIPK3 sponges miR-558 to suppress heparanase expression in bladder cancer cells.

Authors - Yawei Li
human

Br J Cancer

Shed Syndecan-1 is involved in chemotherapy resistance via the EGFR pathway in colorectal cancer.

Authors - X Wang
ratIHC

Neural Regen Res

Reducing LncRNA-5657 expression inhibits the brain inflammatory reaction in septic rats.

Authors - Yi-An Zhan
mouseWB

Diabetes Res Clin Pract

Heparanase-driven inflammation from the AGEs-stimulated macrophages changes the functions of glomerular endothelial cells.

Authors - Guang Xu
humanIHC, WB

Exp Ther Med

MicroRNA-219a-2-3p modulates the proliferation of thyroid cancer cells via the HPSE/cyclin D1 pathway.

Authors - Chuanjia Yang

Reviews

The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.


FH

Fabio Henrique (Verified Customer) (01-17-2019)

Figure 1. IF of HPSE (red) and CD68 (green) in 3D coculture of C4-2B and primary human macrophages. C4-2B and primary human macrophages were encapsulated in a 3D hydrogel, composed of hyaluronic acid and collagen type 1, and cocultured for 5 days. On day 5, cells were fixed in 4% paraformaldehyde for 10 minutes, washed with PBSTritonX 0.3% for 3x 5min and blocked in PBS 10% Goat serum, 1% BSA, for 1 hr at RT. Anti-HPSE was used at 1:100 in blocking buffer, overnight incubation at 4*C. Secondary antibodies AlexaFluor 488 and 568 were used at 1:500 for 1 hr at RT. Imaged using a Nikon A1 confocal microscope. Figure 2: HPSE (red) and CD68 (green) in Grade 3 Endometrial cancer tissue (Frozen). Staining was performed as described above, except secondary antibodies were used at 1:1000. This antibody did not perform well in WB (data not shown).

  • Applications: Immunofluorescence,
  • Primary Antibody Dilution: 1:100
  • Cell Tissue Type: C4-2B and Primary Macrophages; Grade 3 Endometrial Cancer tissue (Frozen)
HPSE Antibody Immunofluorescence, validation (1:100 dilution) in C4-2B and Primary Macrophages; Grade 3 Endometrial Cancer tissue (Frozen) (Cat no:24529-1-AP)