LZTR1 antibody

Catalog No. ABIN2461800

This anti-LZTR1 antibody is a Rabbit Polyclonal antibody detecting LZTR1 in WB and ELISA. Suitable for Human, Mouse, Rat and Dog.

Quick Overview for LZTR1 antibody (ABIN2461800)

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

Reactivity: Human, Mouse, Rat, Dog

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LZTR1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-LZTR1 Antibody

Purification: Antibody is purified by protein A chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LZTR1.

Application Details

Application Notes: LZTR1 antibody can be used for detection of LZTR1 by ELISA at 1:312500. LZTR1 antibody can be used for detection of LZTR1 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store LZTR1 antibody at -20 °C.

Target Details for LZTR1

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

Alternative Name: LZTR1

Background: Leucine-zipper-like transcriptional regulator 1 (LZTR1) is belived to be a DNA-binding protein and transcriptional regulator based on its predicted structural characteristics. The transcript is present in several essential fetal organs and is hemizygously deleted in some DiGeorge syndrome patients. LZTR1 is thought to play a critical role in embryogenesis.Leucine-zipper-like transcriptional regulator 1 is belived to be a DNA-binding protein and transcriptional regulator based on its predicted structural characteristics. The transcript is present in several essential fetal organs and is hemizygously deleted in some DiGeorge syndrome patients. It is thought to play a critical role in embryogenesis.

Molecular Weight: 95 kDa

Gene ID: 8216

NCBI Accession: NP_006758

UniProt: Q8N653