Full Product Name
Rabbit Polyclonal to Human SCN1B
Product Synonym Names
Anti-SCN1B Antibody (N-Terminus) IHC-plus; SCN1B; GEFS+1; Sodium channel subunit beta-1; GEFSP1; Sodium channel beta-1 subunit; Human SCN1B
Product Gene Name
anti-SCN1B antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q07699
Species Reactivity
Human, Mouse, Rat
Purity/Purification
Immunoaffinity Purified
Form/Format
5 mg BSA, 0.9 mg sodium chloride, 0.2 mg sodium phosphate, 0.05 mg Thimerosal, 0.05 mg sodium azide
Concentration
1 mg/ml (lot specific)
Immunogen Description
Synthetic peptide corresponding to a sequence at the N-terminal of human SCN1B, identical to the related rat and mouse sequence.
Immunogen Type
Synthetic peptide
Immunogen
SCN1B antibody was raised against synthetic peptide corresponding to a sequence at the N-terminal of human SCN1B, identical to the related rat and mouse sequence.
Antigen Modification
N-Terminus
Preparation and Storage
Short term +4 degree C; Long term -20 degree C
Other Notes
Small volumes of anti-SCN1B antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-SCN1B antibody
Scn1b encodes one type of beta subunit found in voltage-gated sodium channels. These channels, composed of one alpha and one or two different beta subunits, mediates changes in cell permeability to sodium ions that are essential for the generation of action potentials. Scn1b protein is comprised of an extracellular N-terminus and a single transmembrane domain. Scn1b is considered an auxiliary subunit that modulates channel gating as well as plasma membrane expression levels.
Product Categories/Family for anti-SCN1B antibody
Subfamily:-Sodium-channel---voltage-gated">Family: Ion Channel
Subfamily: Sodium channel - voltage-gated
Applications Tested/Suitable for anti-SCN1B antibody
Immunohistochemistry (IHC - Paraffin), Western Blot (WB)
Application Notes for anti-SCN1B antibody
IHC-P (5 ug/ml), WB
Immunohistochemistry (IHC) of anti-SCN1B antibody
Human Brain, Cortex: Formalin-Fixed, Paraffin-Embedded (FFPE)

Western Blot (WB) of anti-SCN1B antibody
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NCBI/Uniprot data below describe general gene information for SCN1B. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001028.1
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NCBI GenBank Nucleotide #
NM_001037.4
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UniProt Primary Accession #
Q07699
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UniProt Secondary Accession #
Q5TZZ4; Q6TN97[Other Products]
UniProt Related Accession #
Q07699[Other Products]
Molecular Weight
30,440 Da
NCBI Official Full Name
sodium channel subunit beta-1 isoform a
NCBI Official Synonym Full Names
sodium channel, voltage-gated, type I, beta subunit
NCBI Official Symbol
SCN1B??[Similar Products]
NCBI Official Synonym Symbols
ATFB13; BRGDA5; GEFSP1
??[Similar Products]
NCBI Protein Information
sodium channel subunit beta-1; sodium channel beta-1 subunit
UniProt Protein Name
Sodium channel subunit beta-1
Protein Family
Sodium channel
UniProt Gene Name
SCN1B??[Similar Products]
UniProt Entry Name
SCN1B_HUMAN
NCBI Summary for SCN1B
Voltage-gated sodium channels are heteromeric proteins that function in the generation and propagation of action potentials in muscle and neuronal cells. They are composed of one alpha and two beta subunits, where the alpha subunit provides channel activity and the beta-1 subunit modulates the kinetics of channel inactivation. This gene encodes a sodium channel beta-1 subunit. Mutations in this gene result in generalized epilepsy with febrile seizures plus, Brugada syndrome 5, and defects in cardiac conduction. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]
UniProt Comments for SCN1B
SCN1B: Crucial in the assembly, expression, and functional modulation of the heterotrimeric complex of the sodium channel. The subunit beta-1 can modulate multiple alpha subunit isoforms from brain, skeletal muscle, and heart. Its association with neurofascin may target the sodium channels to the nodes of Ranvier of developing axons and retain these channels at the nodes in mature myelinated axons. Defects in SCN1B are the cause of generalized epilepsy with febrile seizures plus type 1 (GEFS+1). Generalized epilepsy with febrile seizures-plus refers to a rare autosomal dominant, familial condition with incomplete penetrance and large intrafamilial variability. Patients display febrile seizures persisting sometimes beyond the age of 6 years and/or a variety of afebrile seizure types. GEFS+ is a disease combining febrile seizures, generalized seizures often precipitated by fever at age 6 years or more, and partial seizures, with a variable degree of severity. Defects in SCN1B are the cause of Brugada syndrome type 5 (BRGDA5). A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs (called ventricular fibrillation), the individual will faint and may die in a few minutes if the heart is not reset. Belongs to the sodium channel auxiliary subunit SCN1B (TC 8.A.17) family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Membrane protein, integral; Channel, sodium
Chromosomal Location of Human Ortholog: 19q13.1
Cellular Component: voltage-gated sodium channel complex; T-tubule; extracellular region
Molecular Function: sodium channel inhibitor activity; sodium channel regulator activity; voltage-gated sodium channel activity
Biological Process: synaptic transmission; membrane depolarization; axon guidance; action potential propagation; corticospinal neuron axon guidance; cell adhesion; locomotion; cardiac muscle contraction; response to pyrethroid
Disease: Generalized Epilepsy With Febrile Seizures Plus, Type 1; Atrial Fibrillation, Familial, 13; Brugada Syndrome 5
Research Articles on SCN1B
1. High SCN1B expression is associated with increased tumour growth and metastasis in breast cancer.
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