Overview |
bs-14125R-HRP |
CXX1 Polyclonal Antibody, HRP Conjugated |
ELISA, IHC-P, IHC-F |
Human |
Specifications |
HRP |
Rabbit |
KLH conjugated synthetic peptide derived from human Cerebral protein 5/CXX1 |
121-209/209 |
Polyclonal |
IgG |
1ug/ul |
Purified by Protein A. |
Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles. |
Target |
8933 |
A6ZKI3 |
Cytoplasm, Cell membrane |
Cerebral protein 5; CAAX box protein 1; CXX 1; FAM127A; Family with sequence similarity 127, member A; Mammalian retrotransposon derived protein 8C; Mar8; MAR8C; Mart8; MART8C; CXX1_HUMAN. |
The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXX1 gene product has been provisionally designated CXX1 pending further characterization. |
Application Dilution |
ELISA |
1:500-1000 |
IHC-P |
1:200-400 |
IHC-F |
1:100-500 |