The ALS2CR11 Antibody (PACO02525) is a high-quality polyclonal antibody designed for research involving ALS2CR11, a protein with a potential role in immune regulation and inflammation. This antibody, raised in rabbits, is highly specific to human samples and is validated for use in a variety of applications, including Western blotting.ALS2CR11 is a protein that may play a crucial role in immune response modulation, making it a valuable target for studies in immunology and cancer research. By binding to the ALS2CR11 protein, this antibody enables researchers to detect and analyze its expression in different cell types, providing valuable insights into its function and potential therapeutic implications.
Understanding the function of ALS2CR11 is essential for advancing our knowledge of immune regulation and inflammation, which are critical factors in various diseases, including cancer, autoimmune disorders, and chronic inflammatory conditions. By utilizing the ALS2CR11 Antibody (PACO02525), researchers can further explore the role of ALS2CR11 in these conditions and potentially uncover new treatment opportunities.
Antibody Name:
ALS2CR11 Antibody
Antibody SKU:
PACO02525
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 ALS2CR11.
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:
ALS2CR11; Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 11 protein
UniProt Protein Function:
ALS2CR11: 2 isoforms of the human protein are produced by alternative splicing.Protein type: Unknown functionChromosomal Location of Human Ortholog: 2q33.1Molecular Function: protein binding
UniProt Protein Details:
NCBI Summary:
An autosomal recessive form of juvenile amyotrophic lateral sclerosis was originally mapped to a region of chromosome 2 that includes this gene. The encoded protein contains a calcium-dependent membrane targeting C2 domain. This domain is often found in proteins that are involved in membrane trafficking and signal transduction. [provided by RefSeq, Jun 2016]
