

Product description
solute carrier family 22 member 18(SLC22A18) Homo sapiens This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region
Source
Rabbit
Applications
WB,IF,ELISA
Reactivity
Human
Dilution
WB: 1/500 - 1/2000. IF: 1/200 - 1/1000. ELISA: 1/10000. Not yet tested in other applications.
Storage
-20°C/1 year
Specificity
ORCTL2 Polyclonal Antibody detects endogenous levels of ORCTL2 protein.
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
The antiserum was produced against synthesized peptide derived from human ORCTL-2. AA range:359-408
Uniprot No
Q96BI1
Alternative names
SLC22A18; BWR1A; BWSCR1A; HET; IMPT1; ITM; ORCTL2; SLC22A1L; TSSC5; Solute carrier family 22 member 18; Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein; Efflux transporter-like protein; Imprinted multi-membrane-spa
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
Background
solute carrier family 22 member 18(SLC22A18) Homo sapiens This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region
Other
Gene_name: SLC22A18 ; Protein_name: Solute carrier family 22 member 18; Expression: Lymph node,Placenta,
Mol.Wt (Da)
14 kD
Concentration
1 mg/ml
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