ARG58620

anti-FGF14 antibody

anti-FGF14 antibody for IHC-Frozen sections,Western blot and Human,Mouse

Overview

Product Description Goat Polyclonal antibody recognizes FGF14
Tested Reactivity Hu, Ms
Predict Reactivity Cow, Rat, Dog, Pig
Tested Application IHC-Fr, WB
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name FGF14
Antigen Species Human
Immunogen Synthetic peptide from the N-terminus of Human FGF14 (NP_034331.2; NP_997550.1). (REQHWDRPSASR-C)
Conjugation Un-conjugated
Alternate Names FHF4; FHF-4; SCA27; Fibroblast growth factor 14; FGF-14; Fibroblast growth factor homologous factor 4

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-Fr1:5000
WB1 - 3 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size ~ 28 kDa

Properties

Form Liquid
Purification Affinity purified
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 14169 Mouse FGF14

GeneID: 2259 Human FGF14

Swiss-port # P70379 Mouse Fibroblast growth factor 14

Swiss-port # Q92915 Human Fibroblast growth factor 14

Gene Symbol FGF14
Gene Full Name fibroblast growth factor 14
Background The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. 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. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]
Function Probably involved in nervous system development and function. [UniProt]
Calculated MW 28 kDa