Product Description

GDPGP1 Polyclonal Antibody

Sizes: 50µl, 100µl

Catalogue Numbers: BS65755-50, BS65755-100

Product: 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Swiss-Prot: Q6ZNW5

Host: Rabbit

Reactivity: Human, Mouse, Rat, Pig, Horse,

Applications: WB

All Applications: WB=1:500-2000

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.

Purification and Purity: affinity purified by Protein A

Storage and Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Specificity: GDPGP1 Polyclonal Antibody detects endogenous levels of GDPGP1 protein.

Bioworld Molecular Weight: 42 kD

Note: For research use only, not for use in diagnostic procedure.

Extra Notes: Primary: Anti-GDPGP1 at 1/1000 dilution

Alternative Name: C15orf58; Chromosome 15 open reading frame 58; GDP-D-glucose phosphorylase 1; GDP-D-glucose phosphorylase C15orf58; gdpgp1; GDPP1_HUMAN; VTC2.聽聽

Immunogen: KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58:301-385/385

Conjugate: Unconjugated

Modification: Unmodified