TXNL4A antibody (AA 1-142)

Catalog No. ABIN6149737

Product Details anti-TXNL4A Antibody

Target: TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Binding Specificity: AA 1-142

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TXNL4A antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: MSYMLPHLHN GWQVDQAILS EEDRVVVIRF GHDWDPTCMK MDEVLYSIAE KVKNFAVIYL VDITEVPDFN KMYELYDPCT VMFFFRNKHI MIDLGTGNNN KINWAMEDKQ EMVDIIETVY RGARKGRGLV VSPKDYSTKY RY

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human TXNL4A (NP_006692.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for TXNL4A

Target: TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Alternative Name: TXNL4A (TXNL4A Products)

Synonyms: Txnl4 antibody, TXNL4A antibody, txnl4a antibody, dim1 antibody, MGC85128 antibody, DIB1 antibody, DIM1 antibody, HsT161 antibody, SNRNP15 antibody, TXNL4 antibody, U5-15kD antibody, D18Wsu98e antibody, Dim1 antibody, ENSMUSG00000057130 antibody, U5-15kDa antibody, thioredoxin-like 4A antibody, thioredoxin like 4A antibody, thioredoxin like 4A S homeolog antibody, Txnl4a antibody, TXNL4A antibody, txnl4a antibody, LOC664328 antibody, txnl4a.S antibody

Background: 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 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.,TXNL4A,BMKS,DIB1,DIM1,SNRNP15,TXNL4,U5-15kD,Cell Biology & Developmental Biology,Apoptosis,TXNL4A

Molecular Weight: 16 kDa

Gene ID: 10907

UniProt: P83876

Pathways: Ribonucleoprotein Complex Subunit Organization