SPINK7 Human

Serine Peptidase Inhibitor Kazal Type 7 Human Recombinant
Cat. No.
BT22345
Source
Escherichia Coli.
Synonyms
Serine peptidase inhibitor Kazal type 7, ECG2, ECRG2, Serine protease inhibitor Kazal-type 7, Esophagus cancer-related gene 2 protein, ECRG-2, SPINK7.
Appearance
Sterile Filtered colorless solution.
Purity
Greater than 85.0% as determined by SDS-PAGE.
Usage
THE BioTek's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
Shipped with Ice Packs
In Stock

Description

SPINK7 Human Recombinant produced in E.coli is a single, non-glycosylated polypeptide chain containing 89 amino acids (20-85) and having a molecular mass of 9.6 kDa.
SPINK7 is fused to a 23 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.

Product Specs

Introduction
Serine peptidase inhibitor Kazal type 7 (SPINK7), containing one Kazal-like domain, is likely a serine protease inhibitor. It is associated with diseases such as esophageal cancer and oral squamous cell carcinoma.
Description
Recombinant human SPINK7, produced in E. coli, is a single, non-glycosylated polypeptide chain comprising 89 amino acids (20-85) with a molecular weight of 9.6 kDa. A 23 amino acid His-tag is fused to the N-terminus. Purification is achieved using proprietary chromatographic techniques.
Physical Appearance
Clear, colorless, and sterile-filtered solution.
Formulation
The SPINK7 solution is provided at a concentration of 0.25 mg/ml in a buffer consisting of 20 mM Tris-HCl (pH 8.0), 0.2 M NaCl, 40% glycerol, and 2 mM DTT.
Stability
For short-term storage (2-4 weeks), the solution should be kept at 4°C. For extended storage, it is recommended to freeze the solution at -20°C. The addition of a carrier protein (0.1% HSA or BSA) is advisable for long-term storage. Repeated freezing and thawing cycles should be avoided.
Purity
The purity of SPINK7 is determined to be greater than 85% by SDS-PAGE analysis.
Synonyms
Serine peptidase inhibitor Kazal type 7, ECG2, ECRG2, Serine protease inhibitor Kazal-type 7, Esophagus cancer-related gene 2 protein, ECRG-2, SPINK7.
Source
Escherichia Coli.
Amino Acid Sequence
MGSSHHHHHH SSGLVPRGSH MGSSEAASLS PKKVDCSIYK KYPVVAIPCP ITYLPVCGSD YITYGNECHL CTESLKSNGR VQFLHDGSC.

Product Science Overview

Introduction

Serine Peptidase Inhibitor Kazal Type 7 (SPINK7), also known as Esophageal Cancer-Related Gene 2 (ECRG2), is a member of the serine protease inhibitor family. This protein is encoded by the SPINK7 gene and is involved in various biological processes, including the regulation of protease activity and the maintenance of epithelial barrier integrity .

Gene and Protein Structure

The SPINK7 gene is located on chromosome 5 and encodes a protein that belongs to the Kazal-type serine protease inhibitor family. The protein structure typically includes a Kazal domain, which is responsible for its inhibitory activity against serine proteases . The recombinant form of SPINK7 is produced using recombinant DNA technology, allowing for its expression and purification in various host systems.

Biological Function

SPINK7 is primarily known for its role as a serine protease inhibitor. It inhibits the activity of serine proteases, which are enzymes that cleave peptide bonds in proteins. This inhibition is crucial for regulating protease activity and preventing excessive proteolysis, which can lead to tissue damage .

Role in Disease

SPINK7 has been implicated in several diseases, most notably esophageal cancer. It was initially identified as a tumor suppressor gene whose expression is often reduced or absent in primary human esophageal cancers . The loss of SPINK7 expression has also been observed in other types of malignancies, suggesting its broader role in cancer biology. Additionally, SPINK7 is involved in the DNA damage response and has been shown to modulate the activity of p53, a key tumor suppressor protein .

Therapeutic Potential

Given its role in cancer and protease regulation, SPINK7 is being explored as a potential therapeutic target. Its ability to inhibit serine proteases makes it a candidate for developing treatments for diseases characterized by excessive protease activity. Furthermore, restoring SPINK7 expression in cancers where it is lost could provide a novel approach to cancer therapy .

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