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Anti-SERPING1 Polyclonal Antibody

Catalog #:   PHC14301 Specific References (49) DATASHEET
Host species: Rabbit
Isotype: IgG
Applications: ELISA, IHC, WB
Accession: P05155
Overview

Catalog No.

PHC14301

Species reactivity

Human

Host species

Rabbit

Isotype

IgG

Clonality

Polyclonal

Immunogen

E. coli - derived recombinant Human SERPING1 (Pro399-Ala500).

Tested applications

ELISA: 1:4000-1:8000, IHC: 1:50-1:100, WB: 1:1000-1:4000

Target

Serpin G1,SERPING1,C1Inh,C1 esterase inhibitor,Plasma protease C1 inhibitor,C1IN,C1 Inh,C1NH,C1-inhibiting factor

Concentration

1.15 mg/ml

Purification

Purified by antigen affinity column.

Accession

P05155

Applications

ELISA, IHC, WB

Form

Liquid

Storage buffer

0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

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.

Data Image
  • WESTERN BLOT
    Recombinant Protein lysates were subjected to SDS PAGE followed by western blot with SERPING1 antibody (PHC14301) at 1 μg/ml.

    Lane 1: Recombinant protein

    Second Ab: Goat Anti-Rabbit IgG H&L Polyclonal antibody, HRP (PTB96431) at 0.1 μg/mL.

    Predict MW: 14 kDa
    Observed MW: 14 kDa
References

Human CD55 Expression and C1 Inhibition Partially Protect Gene-Edited Pig Red Blood Cells From Human Complement-Mediated Hemolysis In Vitro., PMID:40492338

Lanadelumab for prevention of attacks of non-histaminergic normal C1 inhibitor angioedema: results from the randomized, double-blind CASPIAN Study and CASPIAN open-label extension., PMID:40469312

Hereditary angioedema plasma proteomics following specific plasma kallikrein inhibition with lanadelumab., PMID:40417315

Angioedema without urticaria: Diagnosis and management., PMID:40380367

Adherence and persistence among patients with hereditary angioedema receiving long-term prophylaxis in the United States., PMID:40300843

16S rRNA and transcriptome analysis revealed the regulatory mechanism of Romboutsia lituseburensis on serum immunoglobulin levels in geese., PMID:40086254

Omics data integration analysis identified new biological insights into chronic antibody-mediated rejection (CAMR)., PMID:39979925

Indirect treatment comparison of lanadelumab and a C1-esterase inhibitor in pediatric patients with hereditary angioedema., PMID:39836016

Angioedema Due to Acquired C1-Inhibitor Deficiency Without Hematological Condition: A Multicenter French Cohort Study of 34 Patients., PMID:39756514

Idiopathic non-mast cell angioedema: Treatment insights from global experts., PMID:39741376

Hereditary angioedema in children: Review and practical perspective for clinical management., PMID:39655944

Hereditary Angioedema Attacks in Patients Receiving Long-Term Prophylaxis: A Systematic Review., PMID:39508959

Initial Experience of Long-Term Prophylaxis with Lanadelumab for Hereditary Angioedema in China: A Clinical Observation Study on Six Patients., PMID:39362190

Angioedema due to Acquired C1-Inhibitor Deficiency Associated With Monoclonal Gammopathies of Undetermined Significance Characteristics of a French National Cohort., PMID:39357560

Elevated C1s/C1-INH in serum and plasma of myasthenia gravis patients., PMID:39255718

Complete Description of the Three Pathways of the Complement System in a Series of 430 Patients with Rheumatoid Arthritis., PMID:39125933

Structural basis for the inhibition of βFXIIa by garadacimab., PMID:39059382

Familial aggregation of diffuse cutaneous systemic sclerosis: Interplay of C1r gene defect, susceptible HLA haplotype and autoantibodies., PMID:38923752

Identifying hub genes in response to ustekinumab and the impact of ustekinumab treatment on fibrosis in Crohn's disease., PMID:38840917

New Therapies for Type 1 and Type 2 Hereditary Angioedema., PMID:38819650

A quantitative systems pharmacology model of plasma kallikrein-kinin system dysregulation in hereditary angioedema., PMID:38734778

The future of therapeutic options for hereditary angioedema., PMID:38679158

Differentiated pattern of complement system activation between MOG-IgG-associated disease and AQP4-IgG-positive neuromyelitis optica spectrum disorder., PMID:38576611

The molecular determinants of classical pathway complement inhibition by OspEF-related proteins of Borrelia burgdorferi., PMID:38552741

Letter to the editor: network meta-analysis for indirect comparison of lanadelumab and berotralstat for the treatment of hereditary angioedema., PMID:38545965

The role of anticomplement therapy in the management of the kidney allograft., PMID:38485664

Repeated attacks of hereditary angioedema in pediatric female., PMID:38404177

Kallikrein inhibitors for angioedema: the progress of preclinical and early phase studies., PMID:38366937

Effect of lanadelumab on attack frequency and QoL in Japanese patients with hereditary angioedema: Report of five cases., PMID:38268496

C1 esterase inhibitor-mediated immunosuppression in COVID-19: Friend or foe?, PMID:38013973

Efficacy and Safety of Rituximab-Based Treatments in Angioedema With Acquired C1-Inhibitor Deficiency., PMID:37844846

Evaluation of the safety and effectiveness of berotralstat for patients with hereditary angioedema: Report of six cases., PMID:37721445

Patient-level indirect treatment comparison of lanadelumab versus pdC1-INH i.v. in hereditary angioedema patients: PATCH study., PMID:37641968

Efficacy and safety of lanadelumab in Japanese patients with hereditary angioedema: A phase 3 multicenter, open-label study., PMID:37574953

Citrullination of C1-inhibitor as a mechanism of impaired complement regulation in rheumatoid arthritis., PMID:37426666

Healthcare utilization of patients with hereditary angioedema treated with lanadelumab and subcutaneous C1-inhibitor concentrate., PMID:37328263

C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency., PMID:36726161

Lanadelumab for the prevention of hereditary angioedema attacks: A real-world UK audit., PMID:36510404

Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency., PMID:36379410

Outer surface lipoproteins from the Lyme disease spirochete exploit the molecular switch mechanism of the complement protease C1s., PMID:36183830

Acquired angioedema: an unusual presentation of haematological malignancy., PMID:36123007

Longitudinal experience with treatment of acquired angioedema using tranexamic acid., PMID:36065111

Targeting thromboinflammation in COVID-19 - A narrative review of the potential of C1 inhibitor to prevent disease progression., PMID:36030710

Autoantibodies against Complement Classical Pathway Components C1q, C1r, C1s and C1-Inh in Patients with Lupus Nephritis., PMID:36012546

C1-inhibitor influence on platelet activation by thrombin receptors agonists., PMID:35996317

Real World treatment patterns of hereditary angioedema with lanadelumab in Germany: A prescription data analysis., PMID:35913113

Therapeutic monoclonal antibodies with a focus on hereditary angioedema., PMID:35787344

The effects of exercise on complement system proteins in humans: a systematic scoping review., PMID:35452398

Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema., PMID:35386643

Datasheet
$ 170
Product specifications
50 μg 170 100 μg 280

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

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Anti-SERPING1 Polyclonal Antibody [PHC14301]
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