LSBio The Immunohistochemistry Antibody Company
  • Home
  • Products
    • Primary Antibodies
    • Secondary Antibodies
    • IHC-plus Antibodies
    • Isotype Control Antibodies
  • Services
    • Immunohistochemistry Studies
    • Tissue Cross-Reactivity Screening
  • Distributors
  • Resources
    • About our Tissue Bank
    • Customer Support
    • How to Buy
    • IHC-plus Protocol
    • LSBio Media
    • Publications
    • Antibody Reports
  • Company
    • About LifeSpan
    • Press Releases
    • Holiday Schedule
    • Contact Us
  • View Cart

Anti-ATP13A2 Antibody (aa147-161) LS-C74409

Ordering

Wt. Vol. Conc. Price
- 100 µl - $415

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal to Mouse ATP13A2
Mouse
IHC
Unconjugated

Details

Mouse ATP13A2
Rabbit
Mouse (tested or 100% immunogen sequence identity)
Polyclonal
Unpurified serum

Applications

IHC

Specificity and Use

ATP13A2 antibody was raised against a synthetic peptide (C-ELHRQEEAKQVLRYY) as part of mouse ATP13A2 protein (aa: 147-161) conjugated to KLH. Percent identity by BLAST analysis: Mouse (100%); Rat, Hamster (87%); Elephant (80%).
aa147-161
Immunohistochemistry shows specific staining for ATPase. Species cross-reactivity: This antiserum is known to react with rat ATPase. Other species have not yet tested.
Suitable for use in Immunohistochemistry.

Packaging

Lyophilized powder. Reconstitute in 100 ul of sterile water. Centrifuge to remove any insoluble material.
100 µl Reconstitute with ddH2O.
For research use only.

About ATP13A2

Q9NQ11 NM_022089 NP_071372.1

ATP13A2 Antibody, HSA9947 Antibody, PARK9 Antibody, RP1-37C10.4 Antibody, Putative ATPase Antibody, ATPase type 13A2 Antibody, CLN12 Antibody, KRPPD Antibody

ATP13A2 belongs to the P-type superfamily of ATPases that transport inorganic cations and other substrates across cell membranes. ATP13A2 has predominantly neuronal expression and transiently transfected cells studies have shown that it is located in lysosomes. Recently a loss-of-function mutation in ATP13A2 has been linked to an autosomal recessive form of early-onset parkinsonism with pyramidal degeneration and dementia.

Requested From: United States
Date Requested: 7/25/2014
Copyright © 2014 LifeSpan BioSciences, Inc. All Rights Reserved