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Recombinant Human SPINK5 Protein, N-His

Catalog #:   YHJ64201 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: Q9NQ38
Protein length: Gly699-Ser976
Overview

Catalog No.

YHJ64201

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Gly699-Ser976

Predicted molecular weight

34.15 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

Q9NQ38

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

Lympho-epithelial Kazal-type-related inhibitor, SPINK5, LEKTI, Serine protease inhibitor Kazal-type 5

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human SPINK5 protein
References

[Clinical feature and genetic analysis of a preterm infant with Netherton syndrome due to variants of SPINK5 gene]., PMID:40372225

Blocking of IL-4/IL-13 Signalling With Dupilumab Results in Restoration of Serum and Cutaneous Abnormalities in Netherton Syndrome., PMID:40344324

Syndromic epidermal differentiation disorders: New classification towards pathogenesis-based therapy., PMID:40184496

Abrocitinib alleviates the symptoms of Netherton syndrome and is well tolerated., PMID:40159127

Finding Potential Drug Targets for Pre-Eclampsia Using Mendelian Randomisation and Colocalisation Analysis., PMID:40028697

Targeting kallikrein proteases for dandruff therapy., PMID:39707892

Plasma Proteome Alterations of Laying Hens Subjected to Heat Stress and Fed a Diet Supplemented with Pequi Oil (Caryocar brasiliense Camb.): New Insights in the Identification of Heat Stress Biomarkers., PMID:39595600

SPINK5 is a key regulator of eosinophil extracellular traps in head and neck squamous cell carcinoma., PMID:39508915

Molecular analysis of inherited disorders of cornification in polish patients show novel variants and functional data and provokes questions on the significance of secondary findings., PMID:39501396

Developing a Core Outcome Set for Netherton Syndrome: An International Multi-Stakeholder e-Delphi Consensus Study., PMID:39496226

Rapid identification of primary atopic disorders (PAD) by a clinical landmark-guided, upfront use of genomic sequencing., PMID:39381601

Malignant Transformation of Normal Oral Tissue to Dysplasia and Early Oral Squamous Cell Carcinoma: An In Silico Transcriptomics Approach., PMID:39376501

Development of a biomarker-based platform for comprehensive skin characterization using minimally invasive skin sampling and quantitative real-time PCR., PMID:39141418

LEKTI domain 6 displays anti-inflammatory action in vitro and in a murine atopic dermatitis model., PMID:38849289

Development of a back-titration assay to quantitate functional lympho-epithelial Kazal-type inhibitors (LEKTI) in skin samples., PMID:38556114

Functional characterization of serine proteinase inhibitor Kazal-Type in the red claw crayfish Cherax quadricarinatus., PMID:38537926

SPINK5 inhibits esophageal squamous cell carcinoma metastasis via immune activity., PMID:38442944

Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review., PMID:38419182

Netherton Syndrome with a Novel Likely Pathogenic Variant c.420del (p.Ser141ProfsTer5) in SPINK5 Gene: A Case Report., PMID:38406644

Comparative analyses of Netherton syndrome patients and Spink5 conditional knock-out mice uncover disease-relevant pathways., PMID:38316920

Translatome profiling reveals Itih4 as a novel smooth muscle cell-specific gene in atherosclerosis., PMID:38289873

Severe Hypernatremia as Presentation of Netherton Syndrome., PMID:38025195

EMT-related gene risk model establishment for prognosis and drug treatment efficiency prediction in hepatocellular carcinoma., PMID:37990105

Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in SPINK5 Gene., PMID:37239440

Clinical and genetic characterization of Netherton syndrome due to SPINK5 founder variant in Latvian population., PMID:37102386

Inhibition of the Tumor Suppressor Gene SPINK5 via EHMT2 Induces the Oral Squamous Cell Carcinoma Development., PMID:37071303

Netherton Syndrome in a Mother and Her Two Children., PMID:36893349

Prevalence of and risk factors for nutritional deficiency and food allergy in a cohort of 21 patients with Netherton syndrome., PMID:36705039

Biological treatments for pediatric Netherton syndrome., PMID:36619513

Weighted gene co-expression network analysis combined with machine learning validation to identify key hub biomarkers in colorectal cancer., PMID:36576616

Dupilumab improves clinical symptoms in children with Netherton syndrome by suppressing Th2-mediated inflammation., PMID:36569942

Dual antibody inhibition of KLK5 and KLK7 for Netherton syndrome and atopic dermatitis., PMID:36516271

Ustekinumab therapy for Netherton syndrome., PMID:36419401

Computational modelling predicts impaired barrier function and higher sensitivity to skin inflammation following pH elevation., PMID:36321871

Treatment of Netherton syndrome with dupilumab., PMID:36321361

Establishment of a mouse model of Netherton syndrome based on CRISPR/Cas9 technology., PMID:36301754

A recombinase polymerase amplification (RPA) combined with strip visualization method for RNA-based presumptive tests of saliva and vaginal secretion., PMID:36265335

Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology., PMID:36183486

Novel splice site mutation at the C-terminal of SPINK5 cause a unique Netherton syndrome phenotype mimicking pustular psoriasis., PMID:36165187

Photoprotective activities of Lignosus rhinocerus in UV-irradiated human keratinocytes., PMID:35987413

Lobelia chinensis Extract and Its Active Compound, Diosmetin, Improve Atopic Dermatitis by Reinforcing Skin Barrier Function through SPINK5/LEKTI Regulation., PMID:35955819

Aberrant serine protease activities in atopic dermatitis., PMID:35817663

The Pathogenesis of Giant Condyloma Acuminatum (Buschke-Lowenstein Tumor): An Overview., PMID:35562936

Genome-wide association study identifies kallikrein 5 in type 2 inflammation-low asthma., PMID:35487308

SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome., PMID:35438212

SPINK5 is a Tumor-Suppressor Gene Involved in the Progression of Nonsmall Cell Lung Carcinoma through Negatively Regulating PSIP1., PMID:35368958

The Lineage Differentiation and Dynamic Heterogeneity of Thymic Epithelial Cells During Thymus Organogenesis., PMID:35273595

A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata., PMID:35178752

SPINK5 is a Prognostic Biomarker Associated With the Progression and Prognosis of Laryngeal Squamous Cell Carcinoma Identified by Weighted Gene Co-Expression Network Analysis., PMID:35140453

Bioinformatics analysis reveals that ANXA1 and SPINK5 are novel tumor suppressor genes in patients with oral squamous cell carcinoma., PMID:35116500

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

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For research use only. Not for human or drug use.

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Recombinant Human SPINK5 Protein, N-His [YHJ64201]
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