Atlastin GTPase 1 (ATL1) ELISA Kits

The protein encoded by ATL1 is a GTPase and a Golgi body transmembrane protein. Additionally we are shipping ATL1 Antibodies (60) and ATL1 Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human ATL1 ATL1 51062 Q8WXF7
Anti-Mouse ATL1 ATL1 73991 Q8BH66
Anti-Rat ATL1 ATL1 362750 Q6PST4
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More ELISA Kits for ATL1 Interaction Partners

Zebrafish Atlastin GTPase 1 (ATL1) interaction partners

  1. This study suggests that atlastin may regulate BMP receptor (show BMPR1A ELISA Kits) trafficking. and genetic or pharmacological inhibition of BMP signaling was sufficient to rescue the loss of mobility and spinal motor axon defects of atl1 morphants.

Human Atlastin GTPase 1 (ATL1) interaction partners

  1. The results suggest that tethering and lipid mixing are catalyzed concurrently by atlastin GTPase (show RACGAP1 ELISA Kits) hydrolysis but that the energy requirement for lipid mixing exceeds that for tethering, and the full energy released through crossover formation is necessary for fusion.

  2. that Atlastin 1 mutations may cause autosomal recessively inherited paraplegia with an underlying loss-of-function mechanism. Hence, patients with recessive forms of HSP should also be tested for the Atlastin 1 gene.

  3. This study showed that the mutations of were detected in SPG11 (show SPG11 ELISA Kits), ATL1, NIPA1 (show NIPA1 ELISA Kits), and ABCD1 (show ABCD1 ELISA Kits) in patient with hereditary spastic paraplegia.

  4. We identified two novel mutations and two previously reported mutations in SPAST (show SPAST ELISA Kits) and ATL1, respectively. The family with the ATL1 c.1204T>G mutation exhibited male-lethality, female infancy-onset, and pseudo- X-linked dominant transmission

  5. Novel splicing pathogenic variants were identified in ATL1 genes of Korean patients with hereditary spastic paraplegia.

  6. a deficit in the membrane fusion activity of atlastin1 may be a key contributor, but is not required, for hereditary spastic paraplegia causation.

  7. These results suggest that the three ATLs have different capacities to mediate endoplasmic reticulum fusion, with ATL1 being the strongest and ATL3 (show ATL3 ELISA Kits) being the weakest.

  8. purified and reconstituted human ATL1 exhibited no in vitro fusion activity. When the cytosolic segment of human ATL1 was connected to the transmembrane (TM) region and C-terminal tail (CT) of Drosophila ATL

  9. Data showed 3 micro-mutations and 2 exon deletions in SPAST (show SPAST ELISA Kits) gene and 2 micro-mutations in ATL1 gene in this cohort of Chinese patients with spastic paraplegia.

  10. Our combined findings show that homozygosity for the ATL1 missense variant remains the only plausible cause of Hereditary spastic paraplegias, whereas heterozygous carriers are asymptomatic.

Mouse (Murine) Atlastin GTPase 1 (ATL1) interaction partners

  1. Endoplasmic reticulum morphology is markedly disrupted in ATL1, ATL2 (show ATL2 ELISA Kits), and ATL3 (show ATL3 ELISA Kits) knockout cells.

  2. VCP (valosin-containing protein (show vcp ELISA Kits)), together with its cofactor P47 (show MFGE8 ELISA Kits) and the endoplasmic reticulum (ER) morphology regulator ATL1 (Atlastin-1), regulates tubular ER formation

  3. This publication discusses functional and mutational aspects of atlastin GTPase 1 in humans.

ATL1 Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with Atlastin GTPase 1 (ATL1) ELISA Kits

  • atlastin GTPase 1 (ATL1) antibody
  • atlastin GTPase 1 (atl1) antibody
  • atlastin GTPase 1 (LOC100347174) antibody
  • atlastin GTPase 1 (Atl1) antibody
  • 4930435M24Rik antibody
  • AD-FSP antibody
  • Adfsp antibody
  • ATL1 antibody
  • atlastin antibody
  • Atlastin-1 antibody
  • atlastin1 antibody
  • fj46c01 antibody
  • Fsp1 antibody
  • GBP3 antibody
  • HSN1D antibody
  • MGC146251 antibody
  • Spg3 antibody
  • Spg3a antibody
  • wu:fj46c01 antibody

Protein level used designations for Atlastin GTPase 1 (ATL1) ELISA Kits

atlastin GTPase 1 , spastic paraplegia 3A (autosomal dominant) , atlastin-1 , atlastin-1-like , GBP-3 , GTP-binding protein 3 , brain-specific GTP-binding protein , guanine nucleotide-binding protein 3 , guanylate-binding protein 3 , hGBP3 , spastic paraplegia 3 protein A , spastic paraplegia 3A homolog

467452 Pan troglodytes
480318 Canis lupus familiaris
571909 Danio rerio
779669 Xenopus (Silurana) tropicalis
100158193 Sus scrofa
100413587 Callithrix jacchus
100347174 Oryctolagus cuniculus
100603089 Nomascus leucogenys
51062 Homo sapiens
73991 Mus musculus
362750 Rattus norvegicus
535424 Bos taurus
100173943 Pongo abelii
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