LZTR1 antibody (N-Term)

Catalog No. ABIN500210

The Rabbit Polyclonal anti-LZTR1 antibody has been validated for WB, IHC (p) and EIA. It is suitable to detect LZTR1 in samples from Human, Mouse and Rat.

Quick Overview for LZTR1 antibody (N-Term) (ABIN500210)

Target: LZTR1 (Leucine-Zipper-Like Transcription Regulator 1 (LZTR1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LZTR1 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Product Details anti-LZTR1 Antibody

Binding Specificity: N-Term

Cross-Reactivity (Details): Species reactivity (tested):Human, mouse, rat

Purification: Peptide affinity chromatography

Immunogen: LZTR1 antibody was raised against a 14 amino acid peptide near the amino terminus of human LZTR1.

Isotype: IgG

Application Details

Application Notes: ELISA. Western blot: 1 - 2 μg/mL. Immunohistochemistry on paraffin sections.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Handling

Concentration: 1.0 mg/mL

Buffer: PBS containing 0.02 % sodium azide

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freezing and thawing.

Storage: -20 °C

Storage Comment: Store the antibody (in aliquots) at -20 °C.

Target Details for LZTR1

Target: LZTR1 (Leucine-Zipper-Like Transcription Regulator 1 (LZTR1))

Alternative Name: LZTR1

Background: LZTR1, a member of the BTB-kelch superfamily, was initially described as a putative transcriptional regulator based on weak homology to members of the basic leucine zipper-like family, the encoded protein subsequently has been shown to localize exclusively to the Golgi network where it may help stabilize the Golgi complex. Deletion of this gene may be associated with DiGeorge syndrome, a developmental field defect involving the third and fourth pharyngeal pouches, causing the absence of thymus and parathyroid glands, congenital cardiac abnormalities and facial dysmorphism. LZTR1 is tyrosine phosphorylated and subsequently degraded upon induction of apoptosis.Synonyms: Leucine zipper-like transcription regulator 1

Gene ID: 8216

UniProt: Q20WK0