Anti-FGF17 Monoclonal Antibody (16B11)

Subcat	Description	Isotype	Antibody Modification	Conjugate	Size	Price	Quantity
ASZ1C739	Anti-FGF17 Antibody (16B11)	Mouse IgG		None		$460		Add

Subcat

Description

Isotype

Antibody Modification

Conjugate

Size

Price

Quantity

ASZ1C739

Anti-FGF17 Antibody (16B11)

Mouse IgG

None

$460

Add

Anti-FGF17 Monoclonal Antibody (16B11)
- Product Description:
  
  The Anti-FGF17 antibody is a mouse monoclonal antibody recommended for immunohistochemistry, immunocytochemistry, western blot, immunoprecipitation and other applications. This antibody specifically targets human FGF17.
  
  Applications:
  
  Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
  
  Source:
  
  Mouse
  
  Target:
  
  FGF17
  
  Target Species:
  
  Human
  
  Specificity:
  
  This antibody reacts with human Fibroblast Growth Factor 17 (FGF17).
  
  Clonality:
  
  Monoclonal
  
  Clone ID:
  
  16B11
  
  Purification:
  
  The antibody was purified by affinity chromatography.
  
  Purity:
  
  >95% as determined by SDS-PAGE
  
  Concentration:
  
  1 mg/mL
  
  Form:
  
  Liquid
  
  Formulation:
  
  Contact us for custom product formulation.
  
  Preservative:
  
  0.02% sodium azide
  
  Shipping:
  
  Shipped at 4°C.
  
  Storage:
  
  This antibody can be stored at 2°C-8°C for one month. For longer storage, store at -20°C. Avoid repeated freeze-thaw cycles.
Anti-FGF17 Monoclonal Antibody (16B11) Applications
- Recommended Dilution:
  
  Western Blot: 1:500-1:5000
  Immunohistochemistry: 1:50-1:200
  Immunocytochemistry: 1:50-1:200
  
  Note:
  
  Optimal dilutions/concentrations should be determined by the end user.

Protein Name

Fibroblast growth factor 17

Introduction

This gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family 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. This protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants.

Alternative Names

FGF-13; FGF-17; HH20

Gene ID

8822

UniProt

O60258

Related Disease

Hypogonadotropic hypogonadism 20 with or without anosmia (HH20)

Subcellular Location

Secreted.

Tissue Specificity

Preferentially expressed in the embryonic brain.

Function

Plays an important role in the regulation of embryonic development and as signaling molecule in the induction and patterning of the embryonic brain. Required for normal brain development.

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