-
Product Name
SCN9A/Nav1.7-Specific antibody
- Documents
-
Description
SCN9A/Nav1.7-Specific Rabbit Polyclonal antibody. Positive WB detected in A431 cells. Positive IF detected in PC-12 cells. Positive IHC detected in human brain tissue. Observed molecular weight by Western-blot: 228kd
-
Tested applications
ELISA, WB, IF, IHC
-
Species reactivity
Human; other species not tested.
-
Alternative names
ETHA antibody; hNE Na antibody; Nav1.7 antibody; NE NA antibody; NENA antibody; NeuroendOCrine sodium channel antibody; Peripheral sodium channel 1 antibody; PN1 antibody; SCN9A antibody
-
Isotype
Rabbit IgG
-
Preparation
This antibody was obtained by immunization of Peptide (Accession Number: NM_002977). Purification method: Antigen affinity purified.
-
Clonality
Polyclonal
-
Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
-
Storage instructions
Store at -20℃. DO NOT ALIQUOT
-
Applications
Recommended Dilution:
WB: 1:500-1:5000
IHC: 1:20-1:200
IF: 1:20-1:200
-
Validations
A431 cells were subjected to SDS PAGE followed by western blot with Catalog No:115008(SCN9A-Specific antibody) at dilution of 1:500
Immunohistochemistry of paraffin-embedded human brain tissue slide using Catalog No:115008(SCN9A-Specific Antibody) at dilution of 1:200 (under 10x lens)
Immunofluorescent analysis of PC-12 cells using Catalog No:115008(SCN9A-Specific Antibody) at dilution of 1:50 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
-
Background
SCN9A, also named as NENA, PN1, ETHA, NE-NA, Nav1.7 and hNE-Na, belongs to the sodium channel family. SCN9A mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, SCN9A forms a sodium-selective channel through which Na+ ions may pass in accordance with their electrochemical gradient. It is a tetrodotoxin-sensitive Na+ channel isoform. SCN9a plays a role in pain mechanisms, especially in the development of inflammatory pain. Defects in SCN9A are the cause of primary erythermalgia or autosomal recessive congenital indifference to pain or paroxysmal extreme pain disorder (PEPD). The antibody is specific to SCN9A
Related Products / Services
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"