Human FGF-13 1B Antibody

Catalog #: AF1909 Datasheet / COA / SDS

Catalog #	Availability	Size / Price	Qty
AF1909
AF1909-SP

All FGF-13 Antibodies

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Summary Preparation and Storage Reconstitution Calculator Background Product Datasheets Related Research Areas

Human FGF-13 1B Antibody Summary

Species Reactivity

Human

Specificity

Detects human FGF-13 1B in direct ELISAs and Western blots. In direct ELISAs, approximately 10% cross-reactivity with recombinant human (rh) FGF-12 is observed and 5% cross-reactivity with rhFGF-11 is observed.

Source

Polyclonal Goat IgG

Purification

Antigen Affinity-purified

Immunogen

E. coli-derived recombinant human FGF-13 isoform 1B
Ala2-Thr192
Accession # Q92913-2

Formulation

Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.

Label

Unconjugated

Applications

Recommended Concentration

Sample

Western Blot

0.1 µg/mL

Recombinant Human FGF‑13 1B

Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.

Reconstitution Calculator

Preparation and Storage

Reconstitution

Reconstitute at 0.2 mg/mL in sterile PBS.

Shipping

Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.

Stability & Storage

Use a manual defrost freezer and avoid repeated freeze-thaw cycles.

12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
6 months, -20 to -70 °C under sterile conditions after reconstitution.

Background: FGF-13

FGF-13, also known as FGF homologous factor 2 (FHF-2), is a member of the FGF family. It is expressed in brain and skeletal muscle and has been implicated in nervous system development and function. The gene for FGF-13 has been localized in human chromosome X, in a region associated with Borjeson-Forssman-Lehmann syndrome, a syndromal X-linked mental retardation. By alternative splicing, two isoforms that differ in their amino-terminal residues have been described.

Long Name

Fibroblast Growth Factor 13

Entrez Gene IDs

2258 (Human)

Alternate Names

FGF13; FGF-13; FGF2Fibroblast growth factor homologous factor 2; FHF2FHF-2; fibroblast growth factor 13