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.
Applications:Suitable for use in Western Blot, Immunofluorescence and ELISA.
Optimal dilutions to be determined by the researcher.
Recommended Dilution:Western Blot: 1:1000Immunofluorescence: 1:10-1:50Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months after receipt.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：200ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by Protein A and peptide affinity chromatography.
Form：Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.
Specificity：Recognizes human SLC11A2. Species Crossreactivity: mouse and rat
Isotype：IgG
Calc Applications Abbrev：E IF WB
Calc Crossreactivity：Hu Mo Rt
Immunogen：KLH-conjugated synthetic peptide mapping to a fragment of residues within amino acids 262-291 in the central region of mouse SLC11A2, UniProt Accession #NP_001167598.1; NP_000608.1; P49281.
