The FOXD4L1 Polyclonal Antibody (PACO02639) is a valuable tool for researchers studying the FOXD4L1 protein, which is involved in transcriptional regulation, cell differentiation, and development. This antibody, raised in rabbits, exhibits high specificity and sensitivity for detecting FOXD4L1 in human samples, making it suitable for a variety of experimental applications, including Western blotting.FOXD4L1 is a transcription factor that plays a crucial role in various biological processes, including embryonic development and tissue differentiation.
Dysregulation of FOXD4L1 has been associated with certain cancers and developmental disorders, highlighting its importance as a potential therapeutic target and biomarker. By using the FOXD4L1 Polyclonal Antibody, researchers can investigate the function and expression of FOXD4L1 in different cell types and tissues, advancing our understanding of its role in health and disease.
Antibody Name:
FOXD4L1 Antibody
Antibody SKU:
PACO02639
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, WB
Recommended Dilutions:
WB:1:500-1:2000
Species Reactivity:
Human
Immunogen:
synthesized peptide derived from the C-terminal region of human FoxD4L1.
Form:
Liquid
Storage Buffer:
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Purification Method:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Non-conjugated
Synonyms:
FOXD4L1; Forkhead box protein D4-like 1; FOXD4-like 1
UniProt Protein Function:
FOXD4L1: Protein type: DNA-bindingChromosomal Location of Human Ortholog: 2q13Cellular Component: nucleus
UniProt Protein Details:
NCBI Summary:
This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found. [provided by RefSeq, Jul 2008]
