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anti-ABHD11 antibody :: Rabbit anti-Human ABHDB Polyclonal Antibody

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Catalog # MBS9207593
Unit / Price
  0.08 mL  /  $150 +1 FREE 8GB USB
  0.4 mL  /  $340 +1 FREE 8GB USB
Product Name

ABHDB (ABHD11), Polyclonal Antibody

Also Known As

ABHDB Antibody (Center)

Product Synonym Names
Alpha/beta hydrolase domain-containing protein 11; Abhydrolase domain-containing protein 11; 3---; Williams-Beuren syndrome chromosomal region 21 protein; ABHD11; WBSCR21
Antibody/Peptide Pairs
ABHDB peptide (MBS9228200) is used for blocking the activity of ABHDB antibody (MBS9207593)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Immunogen Sequence Positions
Immunogen Sequence Length
3D Structure
ModBase 3D Structure for Q8NFV4
Rabbit Ig
Species Reactivity
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.
Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Vial Concentration: 0.5 (lot specific)
Antigen Type
Synthetic Peptide
Antigen Source
Preparation and Storage
Maintain refrigerated at 2-8 degree C for up to 6 months. For long term storage store at -20 degree C in small aliquots to prevent freeze-thaw cycles.
Other Notes
Small volumes of anti-ABHD11 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-ABHD11 antibody
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.
Applications Tested/Suitable for anti-ABHD11 antibody
Western Blot (WB), ELISA (EIA), Flow Cytometry (FC/FACS)
Application Notes for anti-ABHD11 antibody

Western Blot (WB) of anti-ABHD11 antibody
Western blot analysis of ABHDB Antibody (Center) in MCF-7 cell line lysates (35ug/lane). ABHDB (arrow) was detected using the purified Pab.
anti-ABHD11 antibody Western Blot (WB) (WB) image
Flow Cytometry (FC/FACS) of anti-ABHD11 antibody
ABHDB Antibody (Center) flow cytometric analysis of MCF-7 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
anti-ABHD11 antibody Flow Cytometry (FC/FACS) (FC/FACS) image
NCBI/Uniprot data below describe general gene information for ABHD11. It may not necessarily be applicable to this product.
NCBI Accession #
NCBI Related Accession #
NCBI GenBank Nucleotide #
UniProt Primary Accession #
UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
NCBI Official Full Name
alpha/beta hydrolase domain-containing protein 11 isoform 8
NCBI Official Synonym Full Names
abhydrolase domain containing 11
NCBI Official Symbol
ABHD11  [Similar Products]
NCBI Official Synonym Symbols
PP1226; WBSCR21
  [Similar Products]
NCBI Protein Information
alpha/beta hydrolase domain-containing protein 11
UniProt Protein Name
Alpha/beta hydrolase domain-containing protein 11
UniProt Synonym Protein Names
Williams-Beuren syndrome chromosomal region 21 protein
Protein Family
UniProt Gene Name
ABHD11  [Similar Products]
UniProt Synonym Gene Names
WBSCR21; Abhydrolase domain-containing protein 11  [Similar Products]
UniProt Entry Name
NCBI Summary for ABHD11
This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
UniProt Comments for ABHD11
ABHD11: ABHD11 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Belongs to the AB hydrolase superfamily. 5 isoforms of the human protein are produced by alternative splicing.

Protein type: Hydrolase; EC 3.-.-.-

Chromosomal Location of Human Ortholog: 7q11.23

Cellular Component: mitochondrion

Molecular Function: hydrolase activity

Biological Process: metabolic process
Product References and Citations for anti-ABHD11 antibody
Tsuritani, K., et al. Genome Res. 17(7):1005-1014(2007)
Wan, D., et al. Proc. Natl. Acad. Sci. U.S.A. 101(44):15724-15729(2004)
Merla, G., et al. Hum. Genet. 110(5):429-438(2002)

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