Products for Research Use Only

GDPGP1 Polyclonal Antibody

CAT: 0384-BS65755-01Size: 50 µLDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0384-BS65755-01Size:50 µL
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Background
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
CAS Number
9007-83-4
Structure Composition
0.01M TBS (pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Product Name Alternative
C15orf58; Chromosome 15 open reading frame 58; GDP-D-glucose phosphorylase 1; GDP-D-glucose phosphorylase C15orf58; gdpgp1; GDPP1_HUMAN; VTC2.
Swiss Prot
Q6ZNW5
Reactivity
Human, Mouse, Rat, Pig, Horse
Immunogen
KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58:301-385/385
Conjugation
Unconjugated
Applications
WB
Dilution
WB=1:500-2000
Purity
Affinity purified by Protein A
Modification
Unmodification
Molecular Weight
42 kD
Storage Conditions
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Notes
For research use only, not for use in diagnostic procedure.
Specificity
GDPGP1 Polyclonal Antibody detects endogenous levels of GDPGP1 protein.
Applications Notes
Primary: Anti-GDPGP1 at 1/1000 dilution
Host or Source
Rabbit