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T-Box 19 antibody (AA 229-448)

The Rabbit Polyclonal anti-T-Box 19 antibody has been validated for WB. It is suitable to detect T-Box 19 in samples from Human.
Catalog No. ABIN6148904

Quick Overview for T-Box 19 antibody (AA 229-448) (ABIN6148904)

Target

See all T-Box 19 (TBX19) Antibodies
T-Box 19 (TBX19)

Reactivity

  • 11
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  • 3
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 11
  • 1
Rabbit

Clonality

  • 9
  • 3
Polyclonal

Conjugate

  • 12
This T-Box 19 antibody is un-conjugated

Application

  • 12
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Western Blotting (WB)
  • Binding Specificity

    • 2
    • 1
    • 1
    • 1
    • 1
    AA 229-448

    Sequence

    PEAISESQHV TYSHLGGWIF SNPDGVCTAG NSNYQYAAPL PLPAPHTHHG CEHYSGLRGH RQAPYPSAYM HRNHSPSVNL IESSSNNLQV FSGPDSWTSL SSTPHASILS VPHTNGPINP GPSPYPCLWT ISNGAGGPSG PGPEVHASTP GAFLLGNPAV TSPPSVLSTQ APTSAGVEVL GEPSLTSIAV STWTAVASHP FAGWGGPGAG GHHSPSSLDG

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 229-448 of human TBX19 (NP_005140.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    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

    T-Box 19 (TBX19)

    Alternative Name

    TBX19

    Background

    This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure.,TBX19,TBS19,TPIT,dJ747L4.1,T-box 19,Epigenetics & Nuclear Signaling,Transcription Factors,TBX19

    Molecular Weight

    48 kDa

    Gene ID

    9095

    UniProt

    O60806
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