Gene: SPTA1
Official Full Name: spectrin alpha, erythrocytic 1provided by HGNC
Gene Summary: This 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]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA13554 | SPTA1 Knockout cell line (AC16) | Human | SPTA1 | 1:3-1:4 | negative | Online Inquiry |
| KOA28994 | SPTA1 Knockout cell line (BEAS-2B) | Human | SPTA1 | 1:3~1:4 | negative | Online Inquiry |
| KOA44431 | SPTA1 Knockout cell line (U-2932) | Human | SPTA1 | 1:2-1:4 | negative | Online Inquiry |
| KOA59809 | SPTA1 Knockout cell line (TPC-1) | Human | SPTA1 | 1:5-1:8 | negative | Online Inquiry |
| KOA75234 | SPTA1 Knockout cell line (NCM460) | Human | SPTA1 | 1:2~1:3 | negative | Online Inquiry |
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