ATL1 antibody (C-Term)

Catalog No. ABIN1537385

Product Details anti-ATL1 Antibody

Target: ATL1 (Atlastin GTPase 1 (ATL1))

Binding Specificity: AA 477-504, C-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ATL1 antibody is un-conjugated

Application: Western Blotting (WB)

Predicted Reactivity: B, Pr, M, Rat

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

Immunogen: 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

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

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

Expiry Date: 6 months

Target Details for ATL1

Target: ATL1 (Atlastin GTPase 1 (ATL1))

Alternative Name: ATL1 (ATL1 Products)

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

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.

Molecular Weight: 63544

Gene ID: 51062

NCBI Accession: NP_001121185, NP_056999, NP_853629

UniProt: Q8WXF7