ABHDB Antibody

Product Specifications

Background

ABHDB encodes a protein containing an alpha/beta hydrolase fold domain. This protein is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.

NCBI Gene ID

83451

Swiss Prot

Q8NFV4

Accession Number

Q8NFV4

Host

Rabbit

Reactivity

Human

Immunogen

This ABHDB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 176-205 amino acids from the Central region of human ABHDB.

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Other

Purification

This antibody is purified through a protein A column, followed by peptide affinity purification.

Concentration

Batch dependent

Buffer

Supplied in PBS with 0.09% (W/V) sodium azide.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Calculated Molecular Weight

35 kDa

Fragment

Rabbit Ig

Symbol

ABHD11

NCBI Official Name

Alpha/beta hydrolase domain-containing protein 11

NCBI Organism

Homo sapiens

Background Reference 01

Tsuritani, K., et al. Genome Res. 17 (7) :1005-1014 (2007)

Background Reference 02

Wan, D., et al. Proc. Natl. Acad. Sci. U.S.A. 101 (44) :15724-15729 (2004)

Background Reference 03

Merla, G., et al. Hum. Genet. 110 (5) :429-438 (2002)

Other Product Names

Alpha/beta hydrolase domain-containing protein 11, Abhydrolase domain-containing protein 11, 3---, Williams-Beuren syndrome chromosomal region 21 protein, ABHD11, WBSCR21