SLC22A5 anticorps (C-Term)
Aperçu rapide pour SLC22A5 anticorps (C-Term) (ABIN2789487)
Antigène
Voir toutes SLC22A5 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- C-Term
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Fonction
- SLC22A5 Antibody - C-terminal region
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Séquence
- 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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Attributs du produit
- This is a rabbit polyclonal antibody against SLC22A5. It was validated on Western Blot.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the C-terminal region of SLC22A5
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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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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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 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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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- 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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Autre désignation
- SLC22A5
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Sujet
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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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Poids moléculaire
- 61kDa
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ID gène
- 6584
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NCBI Accession
- NP_003051
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UniProt
- O76082
Antigène
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