SLC25A20 Antikörper (C-Term)
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- Target Alle SLC25A20 Antikörper anzeigen
- SLC25A20 (Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
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Bindungsspezifität
- C-Term
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Reaktivität
- Maus, Human, Ratte, Rind (Kuh), Schaf, Hund, Meerschweinchen, Pferd, Kaninchen, Zebrafisch (Danio rerio)
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SLC25A20 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Sequenz
- 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%
- Produktmerkmale
- This is a rabbit polyclonal antibody against SLC25A20. It was validated on Western Blot using a cell lysate as a positive control.
- Aufreinigung
- Affinity Purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human SLC25A20
- Top Product
- Discover our top product SLC25A20 Primärantikörper
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- Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
- Kommentare
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Antigen size: 301 AA
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- 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." in: Journal of inherited metabolic disease, Vol. 30, Issue 5, pp. 815, (2007) (PubMed).
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Prospective treatment in carnitine-acylcarnitine translocase deficiency." in: Journal of inherited metabolic disease, Vol. 30, Issue 5, pp. 815, (2007) (PubMed).
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- Target
- SLC25A20 (Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
- Andere Bezeichnung
- SLC25A20 (SLC25A20 Produkte)
- Synonyme
- 5848 antikoerper, BG:DS02740.15 antikoerper, CACT antikoerper, CG5848 antikoerper, Cact antikoerper, Dmel\\CG5848 antikoerper, cac antikoerper, dip6 antikoerper, fs(2)ltoRN48 antikoerper, n(2)k17003 antikoerper, cact antikoerper, dif-1 antikoerper, SLC25A20 antikoerper, DKFZp468F1219 antikoerper, zgc:77760 antikoerper, PRKAR2A antikoerper, CAC antikoerper, 1110007P09Rik antikoerper, C78826 antikoerper, mCAC antikoerper, cactus antikoerper, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 antikoerper, solute carrier family 25 member 20 antikoerper, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 L homeolog antikoerper, solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 antikoerper, cact antikoerper, slc25a20 antikoerper, SLC25A20 antikoerper, Slc25a20 antikoerper, slc25a20.L antikoerper
- Hintergrund
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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 - Molekulargewicht
- 33 kDa
- Gen-ID
- 788
- NCBI Accession
- NM_000387, NP_000378
- UniProt
- P97521
- Pathways
- T-Zell Rezeptor Signalweg, Production of Molecular Mediator of Immune Response, Maintenance of Protein Location, Toll-Like Receptors Cascades
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