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TXNL4A antibody (AA 1-142)

This Rabbit Polyclonal antibody specifically detects TXNL4A in WB. It exhibits reactivity toward Human.
Catalog No. ABIN6149737

Quick Overview for TXNL4A antibody (AA 1-142) (ABIN6149737)

Target

See all TXNL4A Antibodies
TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Reactivity

  • 8
  • 2
  • 1
Human

Host

  • 7
  • 1
Rabbit

Clonality

  • 7
  • 1
Polyclonal

Conjugate

  • 4
  • 2
  • 1
  • 1
This TXNL4A antibody is un-conjugated

Application

  • 5
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    AA 1-142

    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 Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • 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

    TXNL4A (Thioredoxin-Like 4A (TXNL4A))

    Alternative Name

    TXNL4A

    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
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