Fibroblast Growth Factor 13 (FGF13) Antibody Pair

Product Graph
1638€ (5 × 96 tests)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
Fibroblast Growth Factor 13 (FGF13) Antibody Pair
category
Antibody Pairs
provider
Abbexa
reference
abx370795
tested applications
ELISA

Description

Fibroblast Growth Factor 13 (FGF13) Antibody Pair for use in Sandwich ELISA assay development.
This antibody pair contains:
Detection: 50 µg
Capture: 200 µg
Standard: 2 µg

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Antibody Pairs
Immunogen Target
Fibroblast Growth Factor 13 (FGF13)
Reactivity
Rat
Assay Data
Sandwich
Assay Type
Capture Antibody: 0.5 mg/ml  Biotin-Conjugated Detection Antibody: 0.2 mg/ml
Reconstitute the standard with Standard Diluent. The volume, and therefore standard concentration, should be determined by the end user.
Recommended Dilution
Dilute the Capture Antibody 125-fold with Coating Buffer.  Dilute the Biotin-Conjugated Detection Antibody 200-fold with Detection Antibody Diluent.  Optimal dilutions/concentrations should be determined by the end user.
Conjugation
Biotin
Size 1
5 × 96 tests
Size 2
10 × 96 tests
Form
Standard form: Lyophilized
Capture Ab: Liquid
Detection Ab: Liquid
Tested Applications
ELISA
Buffer
The Capture and Detection Antibody both contain 0.1% sodium azide.
Availability
Please enquire.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q9ERW3
Gene ID
84488
Background
Antibody pair for FGF13
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

Related Products

FNab03090

FGF13 antibody

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. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.

Ver Producto
P2030

Recombinant Human FGF13

Ver Producto
P6340

Recombinant Human FGF13

Ver Producto