SLC22A5 antibody (C-Term)
Quick Overview for SLC22A5 antibody (C-Term) (ABIN2789486)
Target
See all SLC22A5 AntibodiesReactivity
Host
Clonality
Conjugate
Application
-
-
Binding Specificity
- C-Term
-
Purpose
- SLC22A5 Antibody - C-terminal region
-
Sequence
- GIVVPSTIFD PSELQDLSSK KQQSHNILDL LRTWNIRMVT IMSIMLWMTI
-
Predicted Reactivity
- Cow: 100%, Dog: 85%, Guinea Pig: 92%, Horse: 100%, Human: 100%, Pig: 100%, Rabbit: 92%, Rat: 92%
-
Characteristics
- This is a rabbit polyclonal antibody against SLC22A5. It was validated on Western Blot.
-
Purification
- Affinity Purified
-
-
-
-
Application Notes
- Optimal working dilution should be determined by the investigator.
-
Comment
-
We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP63404-100UG
-
Restrictions
- For Research Use only
-
-
-
Format
- Liquid
-
Concentration
- 0.5 mg/mL
-
Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
-
Preservative
- Sodium azide
-
Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Handling Advice
- prevent freeze-thaw cycles
-
Storage
- 4 °C,-20 °C
-
Storage Comment
- 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.
-
-
- SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
-
Alternative Name
- SLC22A5
-
Background
-
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.
Gene Name: Solute carrier family 22 (organic cation/carnitine transporter), member 5
Alternative Symbols: CDSP, OCTN2
Protein Name: Solute carrier family 22 member 5
-
Molecular Weight
- 61kDa
-
Gene ID
- 6584
-
NCBI Accession
- NP_003051
-
UniProt
- O76082
Target
-