Products for Research Use Only

Recombinant Human FGF13

CAT: 0710-P6340-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0710-P6340-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Product Name Alternative
FGF 13, FGF 2, FGF-13, FGF13, FGF13_HUMAN, FGF2, FHF 2, FHF-2, FHF2, Fibroblast growth factor 13, Fibroblast growth factor homologous factor 2, OTTHUMP00000024143, OTTHUMP00000024144
UniProt
Q92913
Expression Region
1-245
Host
E.Coli
Tag
N-terminal His Tag or N-terminal His-IF2DI Tag, determined during production process
Applications
Western Blot, ELISA
Field of Research
Signal Transduction, Cardiovascular, Immunology, Developmental biology, Neuroscience
Purity
Greater than 90% as determined by SDS-PAGE.
Form
Lyophilized powder
Reconstitution
Centrifuge the vial before opening, reconstitute in sterile distilled water to a concentration of 0.1-1 mg/ml by gently pipetting 2-3 times, don't vortex.
Molecular Weight
26.8 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
The lyophilized protein is stable at -20 °C for up to 1 year. For extended storage, it is recommended to further dilute in working aliquots after reconstitution. The protein solution is stable at ≤ -20 °C for 3 months, or 2-7 days at 2-8 °C under sterile conditions.Avoid repeated freeze/thaw cycle.
Formulation
Lyophilized from a 0.2 μm filtered solution of 10 mM Hepes, 150 mM NaCl with 5% trehalose, pH 7.4.
Organism Species
Human

UniProtKB · Q92913

Fibroblast growth factor 13

FGF13_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q92913
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
FGF13
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
FGF-13
EC number
—
Processing
—
Secondary accessions
B1AK18, B7Z4M7, B7Z8N0, D3DWH4, O95830, Q9NZH9, Q9NZI0
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

Cell membraneCell projectionCytoplasmMembraneMicrotubuleNucleus

Disease

Disease variantEpilepsyIntellectual disability

Biological process

Neurogenesis

PTM

Phosphoprotein