This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogène
This SLC11A2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 262-291 amino acids from the Central region of human SLC11A2.
SLC11A2
Reactivité: Peanut, Plantes
ELISA, IF (cc), IF (p), IHC (p), IHC (fro), ICC
Hôte: Lapin
Polyclonal
unconjugated
Indications d'application
For WB starting dilution is: 1:2000
For IF starting dilution is: 1:10~50
Restrictions
For Research Use only
Format
Liquid
Concentration
0.5 mg/mL
Buffer
Supplied in PBS with 0.09 % (W/V) sodium azide.
Agent conservateur
Sodium azide
Précaution d'utilisation
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Stock
4 °C,-20 °C
Stockage commentaire
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Antigène
SLC11A2
(Solute Carrier Family 11 (Proton-Coupled Divalent Metal Ion Transporters), Member 2 (SLC11A2))
anticorps DCT1, anticorps DMT1, anticorps NRAMP2, anticorps Nramp2, anticorps mk, anticorps van, anticorps Dmt1, anticorps ATNRAMP2, anticorps F8G22.4, anticorps F8G22_4, anticorps NRAMP metal ion transporter 2, anticorps dct1, anticorps dmt1, anticorps nramp2, anticorps SLC11A2, anticorps cb426, anticorps fa07b10, anticorps wu:fa07b10, anticorps zgc:136699, anticorps solute carrier family 11 member 2, anticorps solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2, anticorps NRAMP metal ion transporter 2, anticorps manganese transport protein, anticorps metal transporter Nramp2, anticorps solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2, anticorps SLC11A2, anticorps Slc11a2, anticorps NRAMP2, anticorps LOC9327403, anticorps slc11a2
Sujet
This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.