TXNL4A Antibody Cat. No.: 13-451
TXNL4A Antibody
Specifications
HOST SPECIES: Rabbit
SPECIES REACTIVITY: Human, Mouse
Recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of IMMUNOGEN: human TXNL4A (NP_006692.1).
TESTED APPLICATIONS: WB
APPLICATIONS: WB: ,1:500 - 1:2000
POSITIVE CONTROL: 1) LO2
2) HeLa
3) Jurkat
4) HL-60
5) Mouse pancreas
6) Mouse kidney
PREDICTED MOLECULAR Observed: 13kDa WEIGHT:
Properties
September 29, 2021 1 https://www.prosci-inc.com/txnl4a-antibody-13-451.html PURIFICATION: Affinity purification
CLONALITY: Polyclonal
ISOTYPE: IgG
CONJUGATE: Unconjugated
PHYSICAL STATE: Liquid
BUFFER: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
STORAGE CONDITIONS: Store at -20˚C. Avoid freeze / thaw cycles.
Additional Info
OFFICIAL SYMBOL: TXNL4A
BMKS, DIB1, DIM1, SNRNP15, TXNL4, U5-15kD, thioredoxin-like protein 4A, DIM1 protein ALTERNATE NAMES: homolog, spliceosomal U5 snRNP-specific 15 kDa protein, thioredoxin-like 4, thioredoxin- like U5 snRNP protein U5-15kD
GENE ID: 10907
USER NOTE: Optimal dilutions for each application to be determined by the researcher.
Background and References
The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both BACKGROUND: the coding region and promoter region of this gene have been associated with Burn- McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants.
ANTIBODIES FOR RESEARCH USE ONLY.
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September 29, 2021 2 https://www.prosci-inc.com/txnl4a-antibody-13-451.html