TXNL4A Antibody Cat. No.: 13-451

TXNL4A Antibody

Specifications

HOST SPECIES: Rabbit

SPECIES REACTIVITY: Human, Mouse

Recombinant fusion 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 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 . 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 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