ATL1 anticorps (C-Term)

N° du produit ABIN1537385

Détail du produit anti-ATL1 anticorps

Antigène: ATL1 (Atlastin GTPase 1 (ATL1))

Épitope: AA 477-504, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ATL1 est non-conjugé

Application: Western Blotting (WB)

Homologie: B, Pr, M, Rat

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This ATL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 477-504 amino acids from the C-terminal region of human ATL1.

Clone: RB36288

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: ATL1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur ATL1

Antigène: ATL1 (Atlastin GTPase 1 (ATL1))

Autre désignation: ATL1 (ATL1 Produits)

Synonymes: anticorps ATL1, anticorps SPG3A, anticorps fj46c01, anticorps wu:fj46c01, anticorps spg3a, anticorps MGC146251, anticorps AD-FSP, anticorps FSP1, anticorps GBP3, anticorps HSN1D, anticorps SPG3, anticorps atlastin1, anticorps 4930435M24Rik, anticorps Adfsp, anticorps Fsp1, anticorps Spg3, anticorps Spg3a, anticorps atlastin, anticorps Atlastin-1, anticorps atlastin GTPase 1, anticorps ATL1, anticorps atl1, anticorps Atl1

Sujet: 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.

Poids moléculaire: 63544

ID gène: 51062

NCBI Accession: NP_001121185, NP_056999, NP_853629

UniProt: Q8WXF7