ARG45726

anti-SPG3A / ATL1 antibody

anti-SPG3A / ATL1 antibody for Flow cytometry,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes SPG3A / ATL1
Tested Reactivity Hu
Tested Application FACS, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name SPG3A / ATL1
Antigen Species Human
Immunogen Synthetic peptide corresponding to middle region of human SPG3A / ATL1.
Conjugation Un-conjugated
Alternate Names ATL1; Atlastin GTPase 1; AD-FSP; SPG3A; FSP1; Guanine Nucleotide-Binding Protein 3; Brain-Specific GTP-Binding Protein; Spastic Paraplegia 3 Protein A; GTP-Binding Protein 3; Atlastin-1; GBP-3; HGBP3; GBP3; SPG3; Spastic Paraplegia 3A (Autosomal Dominant); Guanylate-Binding Protein 3; EC 3.6.5.-; Atlastin1; Atlastin; HSN1D

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
IHC-P2-5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 64 kDa

Properties

Form Liquid
Purification Affinity purified
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
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: 51062 Human ATL1

Swiss-port # Q8WXF7 Human Atlastin-1

Gene Symbol ATL1
Gene Full Name Atlastin GTPase 1
Background The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Function GTPase tethering membranes through formation of trans-homooligomers and mediating homotypic fusion of endoplasmic reticulum membranes. Functions in endoplasmic reticulum tubular network biogenesis. [UniProt]
Cellular Localization Cell projection; Endoplasmic reticulum; Golgi apparatus; Membrane. [UniProt]
Calculated MW 64 kDa
PTM Acetylation; Phosphoprotein. [UniProt]