ABHD11 Antibody

Code CSB-PA973412
Size US$297
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  • Western blot analysis of extracts from HUVEC cells and COLO cells, using ABHD11 antibody.
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) ABHD11 Polyclonal antibody
Uniprot No.
Target Names
ABHD11
Alternative Names
ABHD11 antibody; WBSCR21 antibody; PP1226Protein ABHD11 antibody; EC 3.-.-.- antibody; Alpha/beta hydrolase domain-containing protein 11 antibody; Abhydrolase domain-containing protein 11 antibody; Williams-Beuren syndrome chromosomal region 21 protein antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Synthesized peptide derived from internal of Human ABHD11.
Immunogen Species
Homo sapiens (Human)
Clonality
Polyclonal
Purification Method
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
It differs from different batches. Please contact us to confirm it.
Form
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Tested Applications
ELISA,WB
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:3000
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Gene References into Functions
  1. The results demonstrate that human ABHD11 and its yeast homolog YGR031W have a pivotal role in the lipid metabolism. PMID: 28465236
  2. ABHD11-AS1 is expressed in gastric cancer tissues and may have a role as a biological marker PMID: 26280398
  3. Abhydrolase domain-containing protein 11 and Esterase D predict the development of distant metastases and the presence of aggressive lung adenocarcinomas. PMID: 21596165
Involvement in disease
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.
Protein Families
AB hydrolase superfamily
Tissue Specificity
Ubiquitously expressed.
Database Links

HGNC: 16407

KEGG: hsa:83451

STRING: 9606.ENSP00000222800

UniGene: Hs.647045

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