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FGF13 antibody (AA 2-18) (Biotin)

The Mouse Monoclonal anti-FGF13 antibody has been validated for WB, IHC and ELISA. It is suitable to detect FGF13 in samples from Human.
Rockland
Catalog No. ABIN7540506
Supplier Product No.: 200-306-w62

Quick Overview for FGF13 antibody (AA 2-18) (Biotin) (ABIN7540506)

Target

See all FGF13 Antibodies
FGF13 (Fibroblast Growth Factor 13 (FGF13))

Reactivity

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Human

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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  • 2
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This FGF13 antibody is conjugated to Biotin

Application

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Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Clone

S235-22
  • Binding Specificity

    • 16
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    AA 2-18

    Supplier Product No.

    200-306-w62

    Supplier

    Rockland

    Purpose

    FGFA/FHFA (pan) Antibody Biotin

    Cross-Reactivity (Details)

    BLAST analysis suggests that it is 94 % identical to mouse, 100 % identical to rat and >80 % identical to FGF12A/FHF1A, FGF14A/FHF4A, and FGF11A/FHF3A.

    Purification

    Anti-FGFA/FHFA (pan) Antibody was purified from concentrated tissue culture supernate by Protein G chromatography.

    Sterility

    Sterile filtered

    Immunogen

    Anti-FGFA/FHFA (pan) Antibody was produced by repeated immunization of mice with a synthetic peptide containing amino acids 2-18 of human FHF2A.

    Isotype

    IgG2b
  • Application Notes

    ELISA_Dilution: 1:10,000

    Immunohistochemistry_Dilution: User Optimized

    Western_Blot_Dilution: 1:1000

    Comment

    Anti-FGFA/FHFA (pan) Biotin Conjugated Antibody is tested for Western Blots, Immunohistochemistry and Immunocytochemistry. Expect a band approximately ~30 kDa on specific lysates or tissues. Does not cross react with FGF13B/FHF2B. Will cross react with FGF12A/FHF1A and FGF14A/FHF4A. Specific conditions for reactivity should be optimized by the end user.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: 50 % (v/v) Glycerol

    Preservative: 0.1 % (w/v) Sodium Azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Expiry Date

    12 months
  • Target

    FGF13 (Fibroblast Growth Factor 13 (FGF13))

    Alternative Name

    FGF13

    Background

    Acidic fibroblast growth factor, AFGF, Beta endothelial cell growth factor, Fibroblast growth factor homologous factor 2A, Fibroblast growth factor 13A, FGF13A, Beta-endothelial cell growth factor, ECGF, ECGFA antibody, ECGFB, FHF-2, FHF2, FHF13, Fibroblast growth factor homologous factor 2, Fibroblast growth factor 13,FGF13(Fibroblast growth factor 13), also called FHF2 is a protein that in humans is encoded by the FGF13 gene. The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF13is a large gene, extending over approximately 200 kb in Xq26.3, and contains at least 7 exons. By cytogenetic, FISH, and database analysis, Gecz et al. (1999) localized the FGF13 gene within a 400-kb duplication interval on chromosome Xq26.3. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. Other areas of interests and use for researchers include cancer, borjeson-forssman-lehmann syndrome, regulation of actin cytoskeleton pathways, apoptosis, GPCR pathways, TGF-Beta pathways, and Rho family GTPase pathways. This gene is located to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.

    Gene ID

    2258

    UniProt

    Q92913

    Pathways

    Regulation of Cell Size
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