TXNL4A Antikörper (AA 1-142)

Produktnummer ABIN6149737

Produktdetails anti-TXNL4A Antikörper

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

Bindungsspezifität: AA 1-142

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TXNL4A Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu TXNL4A

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

Andere Bezeichnung: TXNL4A (TXNL4A Produkte)

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

Hintergrund: 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

Molekulargewicht: 16 kDa

Gen-ID: 10907

UniProt: P83876

Pathways: Ribonucleoprotein Complex Subunit Organization