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anti-Major Facilitator Superfamily Domain Containing 8 (MFSD8) Antibodies

MFSD8 encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Additionally we are shipping and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
MFSD8 256471 Q8NHS3
Anti-Mouse MFSD8 MFSD8 72175 Q8BH31
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Top anti-Major Facilitator Superfamily Domain Containing 8 Antibodies at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated WB WB Suggested Anti-MFSD8 Antibody Titration: 0.2-1 ug/mlELISA Titer: 1:312500Positive Control: HepG2 cell lysate WB Suggested Anti-MFSD8  Antibody Titration: 0.2-1 µg/mL ELISA Titer: 1:.12500  Positive Control: HepG2 cell lysate 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit Un-conjugated WB Western Blot showing MFSD8 antibody used at a concentration of 1-2 ug/ml to detect its target protein. 50 μg Log in to see 7 to 9 Days
$473.93
Details

MFSD8 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human


More Antibodies against Major Facilitator Superfamily Domain Containing 8 Interaction Partners

Human Major Facilitator Superfamily Domain Containing 8 (MFSD8) interaction partners

  1. MFSD8 genetic testing should also be considered in patients with Rett like phenotype at onset and negative MECP2 (show MECP2 Antibodies) mutation

  2. A mutation in MFSD8, c.472G>A (p.Gly158Ser), segregates with the disease phenotype in variant late infantile neuronal ceroid lipofuscinosis (show CLN6 Antibodies).

  3. In this study, we identified variants in MFSD8 as a novel cause of nonsyndromic autosomal recessive macular dystrophy with central cone involvement.

  4. This study showed that Gene disruption of Mfsd8 provides animal model for CLN7 disease.

  5. Expression and lysosomal targeting of CLN7 are reported.

  6. MFSD8 gene is involved in late-infantile-onset neuronal ceroid lipofuscinose;it was mapped to chromosome 4q28.1-q28.2.

  7. Results describe a novel mutation in the MFSD8 gene, responsible for neuronal ceroid lipofuscinoses, in a consanguineous Egyptian family

  8. Study contributes to a better molecular characterization of Italian NCL (show CLN5 Antibodies) cases, and will facilitate medical genetic counseling in such families.

  9. CLN7/MFSD8 defects are not restricted to the Turkish population, as initially anticipated, but are a relatively common cause of NCL (show CLN5 Antibodies) in different populations.

  10. Data show that neuronal ceroid lipofuscinosis (show CLN6 Antibodies) in a Saudi family is due to a homozygous novel mutation in the most recently described NCL (show CLN5 Antibodies) gene (MFSD8).

Major Facilitator Superfamily Domain Containing 8 (MFSD8) Antigen Profile

Protein Summary

This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile-onset neuronal ceroid lipofuscinoses (vLINCL).

Gene names and symbols associated with MFSD8

  • major facilitator superfamily domain containing 8 (MFSD8) antibody
  • major facilitator superfamily domain containing 8 (Mfsd8) antibody
  • major facilitator superfamily domain containing 8 (mfsd8) antibody
  • 2810423E13Rik antibody
  • AI836898 antibody
  • AV142426 antibody
  • Cln7 antibody

Protein level used designations for MFSD8

ceroid-lipofuscinosis neuronal protein 7 , ceroid-lipofuscinosis, neuronal 7, late infantile , major facilitator superfamily domain-containing protein 8

GENE ID SPECIES
256471 Homo sapiens
72175 Mus musculus
444062 Xenopus laevis
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