IHC-P analysis of human pancreas tissue section using GTX02715 alpha 1 Spectrin antibody [SPTA1/2939R].
![IHC-P analysis of human pancreas tissue section using GTX02715 alpha 1 Spectrin antibody [SPTA1/2939R].](https://www.genetex.com/upload/website/prouct_img/normal/GTX02715/GTX02715_20210319_IHC-P_w_23053122_320.webp "IHC-P analysis of human pancreas tissue section using GTX02715 alpha 1 Spectrin antibody [SPTA1/2939R].")
![WB analysis of K562 whole cell lysate using GTX02715 alpha 1 Spectrin antibody [SPTA1/2939R].](https://www.genetex.com/upload/website/prouct_img/normal/GTX02715/GTX02715_20210319_WB_w_23053122_737.webp "WB analysis of K562 whole cell lysate using GTX02715 alpha 1 Spectrin antibody [SPTA1/2939R].")
IHC-P analysis of human pancreas tissue section using GTX02715 alpha 1 Spectrin antibody [SPTA1/2939R].
alpha 1 Spectrin antibody [SPTA1/2939R]
GTX02715
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetSPTA1
Overview
- SupplierGeneTex
- Product Namealpha 1 Spectrin antibody [SPTA1/2939R]
- Delivery Days Customer9
- ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDSPTA1/2939R
- Concentration200 ug/ml
- ConjugateUnconjugated
- Gene ID6708
- Target nameSPTA1
- Target descriptionspectrin alpha, erythrocytic 1
- Target synonymsalpha-I spectrin; EL2; elliptocytosis 2; erythroid alpha-spectrin; HPP; HS3; spectrin alpha chain, erythrocyte; spectrin alpha chain, erythrocytic 1; SPH3; SPTA
- HostRabbit
- IsotypeIgG
- Scientific DescriptionThis gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [provided by RefSeq, Aug 2017]
- ReactivityHuman
- Storage Instruction2°C to 8°C
- UNSPSC12352203