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Recombinant Human SPTBN4 Protein, N-His

Catalog #:   YHJ55301 Specific References (24) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: Q9H254
Protein length: Lys64-Ser285
Overview

Catalog No.

YHJ55301

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Lys64-Ser285

Predicted molecular weight

28.08 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

Q9H254

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

Beta-IV spectrin, KIAA1642, SPTBN3, Spectrin, non-erythroid beta chain 3, SPTBN4, Spectrin beta chain, non-erythrocytic 4

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human SPTBN4 protein
References

Advancing Personalized Medicine in Alzheimer's Disease: Liquid Biopsy Epigenomics Unveil APOE ε4-Linked Methylation Signatures., PMID:40244264

βIV spectrin abundancy, cellular distribution and sensitivity to AKT/GSK3 regulation in schizophrenia., PMID:39920295

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features., PMID:39371122

Postsynaptic β1 spectrin maintains Na+ channels at the neuromuscular junction., PMID:38441922

Beta IV spectrin inhibits the metastatic growth of melanoma by suppressing VEGFR2-driven tumor angiogenesis., PMID:37680049

Endothelial tip/stalk cell selection requires BMP9-induced βIV-spectrin expression during sprouting angiogenesis., PMID:37126382

Spectrins: molecular organizers and targets of neurological disorders., PMID:36697767

Bioinformatic Analysis of Plus Gene Expression Related to Progression from Leukoplakia to Oral Squamous Cell Carcinoma., PMID:36444596

SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures., PMID:35782384

Loss of β4-spectrin impairs Nav channel clustering at the heminode and temporal fidelity of presynaptic spikes in developing auditory brain., PMID:35393465

Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy-A Case Report., PMID:33986717

Heterozygous variants in SPTBN1 cause intellectual disability and autism., PMID:33847457

Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum., PMID:33772159

Tbx5 variants disrupt Nav1.5 function differently in patients diagnosed with Brugada or Long QT Syndrome., PMID:33576403

Genome-Wide Profiling of Human Papillomavirus DNA Integration into Human Genome and Its Influence on PD-L1 Expression in Chinese Uygur Cervical Cancer Women., PMID:32411801

A novel homozygous splice-site mutation in the SPTBN4 gene causes axonal neuropathy without intellectual disability., PMID:31857255

Detection of a Frameshift Deletion in the SPTBN4 Gene Leads to Prevention of Severe Myopathy and Postnatal Mortality in Pigs., PMID:31850074

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance., PMID:31230720

βIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy., PMID:29861105

Transcriptome analysis reveals enrichment of genes associated with auditory system in swimbladder of channel catfish., PMID:29738887

Expanding the genetic heterogeneity of intellectual disability., PMID:28940097

Postnatal Development of Spasticity Following Transgene Insertion in the Mouse βIV Spectrin Gene (SPTBN4)., PMID:28582869

A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness., PMID:28540413

DNA methylation map of mouse and human brain identifies target genes in Alzheimer's disease., PMID:24030951

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

Contact Information

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Distributor list

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

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Recombinant Human SPTBN4 Protein, N-His [YHJ55301]
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