epitope mapping within an internal region of SLC12A8 of human origin
Modification Notes
SLC12A8 (solute carrier family 12 member 8) is a 714 amino acid multi-pass membrane protein that belongs to the SLC12A transporter family. The SLC12A8 protein is nearly ubiquitously expressed with very low level in normal skin, and highest levels in small intestine, stomach, testis, thyroid and colon. SLC12A8 is a cation/chloride cotransporter that may play a role in the control of keratinocyte proliferation. The SLC12A8 protein shows homology to Na/K/Cl cotransporters, a family of membrane proteins responsible for electroneutral ion transport across a variety of cell types. It has been suggested that SLC12A8 could be identified as a candidate gene for psoriasis susceptibility. SLC12A8 is retinoid responsive. Existing as five alternatively spliced isoforms, the SLC12A8 gene is conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito and C.elegans, and maps to human chromosome 3q21.2. The SLC12A8 gene contains 13 exons and spans over 100 kb.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of SLC12A8 of human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of SLC12A8 of human origin
Tissue Specificity
epitope mapping within an internal region of SLC12A8 of human origin