Transmembrane Protein 126A Protéines (TMEM126A)

The protein encoded by TMEM126A is a mitochondrial membrane protein of unknown function. De plus, nous expédions TMEM126A Kits (10) et et beaucoup plus de produits pour cette protéine.

afficher tous les protéines Gène GeneID UniProt
TMEM126A 66271 Q9D8Y1
Rat TMEM126A TMEM126A 293113 Q5HZA9
TMEM126A 84233 Q9H061
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Showing 3 out of 3 products:

Catalogue No. Origin Source Conjugué Images Quantité Fournisseur Livraison Prix Détails
Cellules d'insectes Souris rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Connectez-vous pour afficher 50 to 55 Days
$5,355.45
Détails
Cellules d'insectes Humain rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Connectez-vous pour afficher 50 to 55 Days
$7,626.01
Détails
HEK-293 Cells Humain Myc-DYKDDDDK Tag Validation with Western Blot 20 μg Connectez-vous pour afficher Disponible
$547.80
Détails

TMEM126A Protéines protéines par origine et source

Origin Exprimée danse Conjugué
Mouse (Murine)

Human ,
,

Plus protéines pour Transmembrane Protein 126A (TMEM126A) partenaires d'interaction

Mouse (Murine) Transmembrane Protein 126A (TMEM126A) interaction partners

  1. TMEM126A contributes to the TLR4 (Montrer TLR4 Protéines) signal up-regulating the expression of genes whose products are involved in antigen presentation.

  2. TMEM126A binds to the extracellular domain of CD137L (Montrer TNFSF9 Protéines) and is detected on cell surface by flow cytometry, cell surface expression of TMEM126A may be essential for CD137L (Montrer TNFSF9 Protéines) reverse signaling.

Human Transmembrane Protein 126A (TMEM126A) interaction partners

  1. TMEM126A is a mitochondrial located mRNA (MLR (Montrer NR3C2 Protéines)) that may be translated in the mitochondrial surface and the protein is subsequently imported to the inner membrane

  2. The p.Arg55X mutation in TMEM126A, homozygous in all affected siblings and heterozygous in both unaffected parents, has been found in a Moroccan family with autosomal recessive optic atrophy.

  3. The first detailed phenotyping of patients with autosomal recessive TMEM126A-associated optic atrophy and auditory neuropathy, is described.

  4. TMEM126A encodes a transmembrane mitochondrial protein (Montrer COX6B2 Protéines) of unknown function, supporting the view that mitochondrial dysfunction may be a hallmark of inherited optic neuropathies including isolated autosomal-recessive forms.

Profil protéine TMEM126A

Profil protéine

The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with TMEM126A

  • transmembrane protein 126A (Tmem126a)
  • transmembrane protein 126A L homeolog (tmem126a.L)
  • transmembrane protein 126A (tmem126a)
  • transmembrane protein 126A (TMEM126A)
  • transmembrane protein 126A (LOC100222067)
  • transmembrane protein 126a (t126a)
  • 1810020E01Rik Protéine
  • MGC64236 Protéine
  • MGC75678 Protéine
  • OPA7 Protéine
  • RGD1305677 Protéine
  • zgc:73348 Protéine

Protein level used designations for TMEM126A

transmembrane protein 126A , Transmembrane protein 126A , transmembrane protein 126a

GENE ID SPECIES
66271 Mus musculus
293113 Rattus norvegicus
379516 Xenopus laevis
393771 Danio rerio
394682 Xenopus (Silurana) tropicalis
426392 Gallus gallus
529762 Bos taurus
608427 Canis lupus familiaris
100174436 Pongo abelii
100196498 Salmo salar
100222067 Taeniopygia guttata
100529013 Ictalurus punctatus
84233 Homo sapiens
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