0 products, total $0.+86-400-890-9989      Login |  Register 中文한국어

Browse By Molecule:

Your Position: Home > Recombinant Protein > Human Cell Expressed > Canine WAP5 / WFDC2 / HE4 Protein

Canine WAP5 / WFDC2 / HE4 Protein PDF Download

Catalog Size (Price) Quantity In Stock Operation Other Information
70012-D02H
  YES          

Protein Production & Purification Service

WAP four-disulfide core domain 2 Protein Datasheet

 

WAP5 / WFDC2 / HE4 Protein Price Inquiry ( Available Sizes )

WAP5 / WFDC2 / HE4 Protein Product Information

Synonym : WFDC2
Protein Construction:

A DNA sequence encoding the canine WFDC2 (Met1-Phe124) was expressed, fused with the Fc region of human IgG1 at the C-terminus.

Source: Canine
Expression Host: Human Cells

WAP5 / WFDC2 / HE4 Protein QC Testing

Purity: > 95% as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

WAP5 / WFDC2 / HE4 protein

Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method
Stability: Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal: Gly 28
Molecular Mass:

The recombinant canine WFDC2/Fc is a disulfide-linked homodimer. The reduced monomer comprises 338 amino acids and has a predicted molecular mass of 37.3 kDa. The apparent molecular mass of the protein is approximately 48 kDa in SDS-PAGE under reducing conditions.

Formulation: Lyophilized from sterile PBS, pH7.4.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
  2. Please contact us for any concerns or special requirements.

WAP5 / WFDC2 / HE4 Protein Usage Guide

Storage: Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

WAP5 / WFDC2 / HE4 Protein Related Products & Topics

Related Areas:

Proteins:

Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
WFDC2/HE4 Human WFDC2/HE4 Protein, Recombinant 12609-H08H
WFDC2/HE4 Canine WAP5 / WFDC2 / HE4 Protein, Recombinant 70012-D02H

Antibodies:

Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
WFDC2/HE4 WB, ELISA WFDC2 / HE4 Antibody 12609-MM15
WFDC2/HE4 WB, ELISA WFDC2 / HE4 Antibody 12609-RP01
WFDC2/HE4 WB, ELISA WFDC2 / HE4 Antibody (Antigen Affinity Purified) 12609-RP02
WFDC2/HE4 WB, ELISA WFDC2/HE4 Antibody, Mouse MAb 12609-R109
WFDC2/HE4 IHC-P WFDC2 / HE4 Antibody 12609-R415

WAP5 / WFDC2 / HE4 Protein Description

WAP four-disulfide core domain protein 2, also known as Epididymal secretory protein E4, Major epididymis-specific protein E4, Putative protease inhibitor WAP5, WFDC2 and HE4, is a secreted protein which contains two WAP domains. WFDC2 / HE4 is a member of a family of stable 4-disulfide core proteins that are secreted at high levels. It is expressed in a number of normal tissues, including male reproductive system, regions of the respiratory tract and nasopharynx. It is highly expressed in a number of tumors cells lines, such ovarian, colon, breast, lung and renal cells lines. Initially described as being exclusively transcribed in the epididymis. WFDC2 may be a component of the innate immune defences of the lung, nasal and oral cavities and suggest that WFDC2 functions in concert with related WAP domain containing proteins in epithelial host defence. WFDC2 re-expression in lung carcinomas may prove to be associated with tumour type and should be studied in further detail. Mammary gland expression of tammar WFDC2 during the course of lactation showed WFDC2 was elevated during pregnancy, reduced in early lactation and absent in mid-late lactation. WFDC2 / HE4 can undergo a complex series of alternative splicing events that can potentially yield five distinct WAP domain containing protein isoforms.

References

  1. Bingle L. et al., 2002, Oncogene. 21 (17): 2768-73.
  2. Hellstr m I. et al., 2003, Cancer Res. 63 (13): 3695-700.
  3. Bingle L. et al., 2006, Respir Res. 7: 61.
  4. Galgano MT. et al., 2006, Mod Pathol.19?(6): 847-53.
  5. Sharp JA. et al., 2007, Evol Dev. 9 (4): 378-92.