LHX4 antibody

Catalog No. ABIN2457952

This Rabbit Polyclonal antibody specifically detects LHX4 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for LHX4 antibody (ABIN2457952)

Target: LHX4 (LIM Homeobox 4 (LHX4))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LHX4 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-LHX4 Antibody

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LHX4.

Application Details

Application Notes: LHX4 antibody can be used for detection of LHX4 by ELISA at 1:12500. LHX4 antibody can be used for detection of LHX4 by western blot at 1 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 50 ?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 LHX4 antibody at -20 °C.

Target Details for LHX4

Target: LHX4 (LIM Homeobox 4 (LHX4))

Alternative Name: LHX4

Background: LHX4 is a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects.This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects. An alternative splice variant has been described but its biological nature has not been determined.

Molecular Weight: 43 kDa

Gene ID: 89884

NCBI Accession: NP_203129

UniProt: P53776