SLC25A20 anticorps (C-Term)
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- Antigène Voir toutes SLC25A20 Anticorps
- SLC25A20 (Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
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Épitope
- C-Term
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Reactivité
- Souris, Humain, Rat, Boeuf (Vache), Mouton, Chien, Cobaye, Cheval, Lapin, Poisson zèbre (Danio rerio)
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SLC25A20 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- GGIAGIFNWA VAIPPDVLKS RFQTAPPGKY PNGFRDVLRE LIRDEGVTSL
- Homologie
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Sheep: 100%, Zebrafish: 93%
- Attributs du produit
- This is a rabbit polyclonal antibody against SLC25A20. It was validated on Western Blot using a cell lysate as a positive control.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the C terminal region of human SLC25A20
- Top Product
- Discover our top product SLC25A20 Anticorps primaire
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- Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
- Commentaires
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Antigen size: 301 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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Prospective treatment in carnitine-acylcarnitine translocase deficiency." dans: Journal of inherited metabolic disease, Vol. 30, Issue 5, pp. 815, (2007) (PubMed).
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Prospective treatment in carnitine-acylcarnitine translocase deficiency." dans: Journal of inherited metabolic disease, Vol. 30, Issue 5, pp. 815, (2007) (PubMed).
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- Antigène
- SLC25A20 (Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
- Autre désignation
- SLC25A20 (SLC25A20 Produits)
- Synonymes
- anticorps 5848, anticorps BG:DS02740.15, anticorps CACT, anticorps CG5848, anticorps Cact, anticorps Dmel\\CG5848, anticorps cac, anticorps dip6, anticorps fs(2)ltoRN48, anticorps n(2)k17003, anticorps cact, anticorps dif-1, anticorps SLC25A20, anticorps DKFZp468F1219, anticorps zgc:77760, anticorps PRKAR2A, anticorps CAC, anticorps 1110007P09Rik, anticorps C78826, anticorps mCAC, anticorps cactus, anticorps solute carrier family 25 (carnitine/acylcarnitine translocase), member 20, anticorps solute carrier family 25 member 20, anticorps solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 L homeolog, anticorps solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20, anticorps cact, anticorps slc25a20, anticorps SLC25A20, anticorps Slc25a20, anticorps slc25a20.L
- Sujet
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SLC25A20 is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space.It mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: CAC, CACT
Protein Interaction Partner: KDM1A, ESR1, UBC, HN1L,
Protein Size: 301 - Poids moléculaire
- 33 kDa
- ID gène
- 788
- NCBI Accession
- NM_000387, NP_000378
- UniProt
- P97521
- Pathways
- TCR Signaling, Production of Molecular Mediator of Immune Response, Maintenance of Protein Location, Toll-Like Receptors Cascades
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