C21orf25 Polyclonal Antibody
Product Specifications
Background
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C2CD2 is an 696 amino acid protien that is secreted. The C2CD2 gene product has been provisionally designated C2CD2 pending further characterization.
Synonyms
C2 calcium-dependent domain containing 2; C2 domain containing protein 2; C21orf25; C21orf258; C2CD2; Chromosome 21 open reading frame 25; MGC71445; TMEM24-like; TMEM24L; CU025_HUMAN.
Gene ID
25966
Host
Rabbit
Cross Reactivity
Human
Immunogen
451-550/696
Target
C21orf25
Clonality
Polyclonal
Isotype
IgG
Conjugation
Unconjugated
Source
KLH conjugated synthetic peptide derived from human C2CD2/C21orf25
Applications
WB, IHC-P, IF (IHC-P)
Purification
Purified by Protein A.
Concentration
1µg/µl
Dilution
WB (1:300-5000), IHC-P (1:200-400), IF (IHC-P) (1:50-200)
Buffer
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
Gene ID URL
25966
Predicted Cross Reactivity
Mouse, Rat, Cow, Sheep, Pig, Horse, Rabbit
Curated Selection
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