SLC22A5 Antikörper (C-Term)
Kurzübersicht für SLC22A5 Antikörper (C-Term) (ABIN2789487)
Target
Alle SLC22A5 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- C-Term
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Verwendungszweck
- SLC22A5 Antibody - C-terminal region
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Sequenz
- TLFLPESFGT PLPDTIDQML RVKGMKHRKT PSHTRMLKDG QERPTILKST
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Homologie
- Cow: 79%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Mouse: 77%, Rat: 86%
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Produktmerkmale
- This is a rabbit polyclonal antibody against SLC22A5. It was validated on Western Blot.
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Aufreinigung
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the C-terminal region of SLC22A5
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Applikationshinweise
- Optimal working dilution should be determined by the investigator.
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Kommentare
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP63405-100UG
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- prevent freeze-thaw cycles
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
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Andere Bezeichnung
- SLC22A5
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Hintergrund
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Background Information: Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy.
Alternative Symbols: CDSP, OCTN2
Protein Name: Solute carrier family 22 member 5
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Molekulargewicht
- 61kDa
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Gen-ID
- 6584
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NCBI Accession
- NP_003051
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UniProt
- O76082
Target
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