ARG59125

anti-ATX2 antibody

anti-ATX2 antibody for Flow cytometry,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes ATX2
Tested Reactivity Hu, Ms, Rat
Predict Reactivity Hm
Tested Application FACS, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name ATX2
Antigen Species Human
Immunogen Synthetic peptide corresponding to aa. 1283-1313 of Human ATX2. (QSALQPIPVSTTAHFPYMTHPSVQAHHQQQL)
Conjugation Un-conjugated
Alternate Names Ataxin-2; ATX2; Trinucleotide repeat-containing gene 13 protein; TNRC13; Spinocerebellar ataxia type 2 protein; ASL13; SCA2

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
IHC-P0.5 - 1 µg/ml
WB0.1 - 0.5 µg/ml
Application Note IHC-P: Antigen Retrieval: Heat mediated was performed in Citrate buffer (pH 6.0) for 20 min.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.9% NaCl, 0.2% Na2HPO4, 0.05% Sodium azide and 5% BSA.
Preservative 0.05% Sodium azide
Stabilizer 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: 20239 Mouse ATXN2

GeneID: 6311 Human ATXN2

Swiss-port # O70305 Mouse Ataxin-2

Swiss-port # Q99700 Human Ataxin-2

Gene Symbol ATXN2
Gene Full Name ataxin 2
Background This gene belongs to a group of genes that is associated with microsatellite-expansion diseases, a class of neurological and neuromuscular disorders caused by expansion of short stretches of repetitive DNA. The protein encoded by this gene has two globular domains near the N-terminus, one of which contains a clathrin-mediated trans-Golgi signal and an endoplasmic reticulum exit signal. The protein is primarily localized to the Golgi apparatus, with deletion of the Golgi and endoplasmic reticulum signals resulting in abnormal subcellular localization. In addition, the N-terminal region contains a polyglutamine tract. Intermediate length expansions of this tract increase susceptibility to amyotrophic lateral sclerosis, while long expansions of this tract result in spinocerebellar ataxia-2, an autosomal-dominantly inherited, neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2015]
Function Involved in EGFR trafficking, acting as negative regulator of endocytic EGFR internalization at the plasma membrane. [UniProt]
Cellular Localization Cytoplasm. [UniProt]
Calculated MW 140 kDa