|Positive WB detected in||COLO 320 cells, mouse thymus tissue, mouse spleen tissue, Raji cells, Jurkat cells|
|Positive IP detected in||Jurkat cells|
|Positive IHC detected in||human lymphoma tissue|
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
|Positive IF detected in||HeLa cells|
|Western Blot (WB)||WB : 1:500-1:3000|
|Immunoprecipitation (IP)||IP : 0.5-4.0 ug for IP and 1:500-1:1000 for WB|
|Immunohistochemistry (IHC)||IHC : 1:50-1:500|
|Immunofluorescence (IF)||IF : 1:50-1:500|
|Sample-dependent, check data in validation data gallery|
12133-2-AP targets TIA1 in WB, IP, IHC, IF, ELISA applications and shows reactivity with human, mouse, rat samples.
|Tested Reactivity||human, mouse, rat|
|Cited Reactivity||chicken, human, mouse, rat|
|Host / Isotype||Rabbit / IgG|
|Immunogen||TIA1 fusion protein Ag2778|
|Full Name||TIA1 cytotoxic granule-associated RNA binding protein|
|Calculated molecular weight||214 aa, 24 kDa, 43 kDa|
|Observed molecular weight||40 kDa|
|GenBank accession number||BC015944|
|Gene ID (NCBI)||7072|
|Purification Method||Antigen affinity purification|
|Storage Buffer||PBS with 0.1% sodium azide and 50% glycerol pH 7.3.|
|Storage Conditions||Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.|
TIA1, also named as p40-TIA-1, is involved in alternative pre-RNA splicing and regulation of mRNA translation by binding to AU-rich elements (AREs) located in mRNA 3' untranslated regions (3' UTRs). It possesses nucleolytic activity against cytotoxic lymphocyte target cells. TIA1 may be involved in apoptosis. Two isoforms of this protein exist - 41kDa and 42kDa. one of these was a missense variant (P362L) in TIA1. Similar to the ALS-related disease proteins TDP-43, hnRNPA1, and FUS, TIA1 is an RNA-binding protein containing a prionlike LCD and assembles into membrane-less organelles, including SGs. Postmortem neuropathology of five TIA1mutations carriers showed a consistent pathological signature with numerous round, hyaline, TAR DNA-binding protein 43 (TDP-43)-positive inclusions.TIA1mutations significantly increased the propensity of TIA1 protein to undergo phase transition. In live cells,TIA1mutations delayed stress granule (SG) disassembly and promoted the accumulation of non-dynamic SGs that harbored TDP-43. Moreover, TDP-43 in SGs became less mobile and insoluble.
|Product Specific Protocols|
|WB protocol for TIA1 antibody 12133-2-AP||Download protocol|
|IHC protocol for TIA1 antibody 12133-2-AP||Download protocol|
|IF protocol for TIA1 antibody 12133-2-AP||Download protocol|
|IP protocol for TIA1 antibody 12133-2-AP||Download protocol|
|Click here to view our Standard Protocols|
Acta Neuropathol Commun
Clinical and neuropathological features of ALS/FTD with TIA1 mutations.
Int J Mol Sci
HuR and TIA1/TIAL1 Are Involved in Regulation of Alternative Splicing of SIRT1 Pre-mRNA.
Int J Mol Med
miR‑335 promotes stress granule formation to inhibit apoptosis by targeting ROCK2 in acute ischemic stroke.
Critical role for G3BP1 in infectious bursal disease virus (IBDV)-induced stress granule formation and viral replication.
Stem Cells Int
Targeted Knockdown of RNA-Binding Protein TIAR for Promoting Self-Renewal and Attenuating Differentiation of Mouse Embryonic Stem Cells.
CLIP: construction of cDNA libraries for high-throughput sequencing from RNAs cross-linked to proteins in vivo.
The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.
Joshua (Verified Customer) (12-28-2019)
PANC1 cells fixed in 4% paraformaldehyde and stained overnight at 4C. Bright staining, mix of nuclear and stress granule localization as expected.
Joshua (Verified Customer) (12-12-2018)
We found acetone fixation (20 min in 100% acetone at -20C) worked better than paraformaldehyde.