LIM Homeobox 4 (LHX4) (Middle Region) Peptide
LHX4
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all LHX4 products
- LHX4 (LIM Homeobox 4 (LHX4))
- Protein Region
- Middle Region
- Origin
- Human
- Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-LHX4 antibody (Catalog #: ARP32424_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- LHX4 (LIM Homeobox 4 (LHX4))
- Synonyms
- LHX4 Peptide, si:dkeyp-35f11.3 Peptide, CPHD4 Peptide, A330062J17Rik Peptide, Gsh-4 Peptide, Gsh4 Peptide, LIM homeobox 4 Peptide, LIM homeobox protein 4 Peptide, LHX4 Peptide, lhx4 Peptide, Lhx4 Peptide
- 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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: Gsh-4, Gsh4, CPHD4
Protein Interaction Partner: IFT172,IFT172
Protein Size: 390 - Molecular Weight
- 43 kDa
- Gene ID
- 89884
- NCBI Accession
- NM_033343, NP_203129
- UniProt
- P53776
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