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ABHD11 Antibody (PACO22109)

SKU:
PACO22109
Product Type:
Antibody
Reactivity:
Human
Host Species:
Rabbit
Isotype:
IgG
Applications:
ELISA
WB
Antibody Type:
Polyclonal Antibody
Conjugation:
Unconjugated
€419
Frequently bought together:

Description

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ABHD11 Antibody (PACO22109)

The ABHD11 Polyclonal Antibody (PAC02209) is a valuable tool for research involving ABHD11, a protein involved in lipid metabolism and cell signaling pathways. This antibody, produced in rabbits, is highly specific to human samples and has been validated for use in Western blot applications. It binds to the ABHD11 protein, allowing for detection and analysis in a variety of cell types, making it ideal for studies in lipid metabolism, signal transduction, and cell biology.ABHD11 is known to play a role in lipid metabolism, specifically in the hydrolysis of lipid substrates, and has been implicated in various diseases, including metabolic disorders and cancer.

Understanding the function and regulation of ABHD11 is important for unraveling its role in these diseases and potentially identifying new therapeutic targets. The ABHD11 Polyclonal Antibody is a reliable tool for researchers seeking to investigate the role of ABHD11 in various cellular processes and disease pathways.

Antibody Name:ABHD11 Antibody (PACO22109)
Antibody SKU:PACO22109
Size:100ul
Host Species:Rabbit
Tested Applications:ELISA, WB
Recommended Dilutions:ELISA:1:2000-1:10000, WB:1:500-1:3000
Species Reactivity:Human
Immunogen:Synthesized peptide derived from internal of human ABHD11.
Form:Liquid
Storage Buffer:Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Purification Method:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Clonality:Polyclonal
Isotype:IgG
Conjugate:Non-conjugated
Product ImageWestern blot analysis of extracts from HUVEC cells and COLO cells, using ABHD11 antibody.
Background: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.
Synonyms:ABHDB; abhydrolase domain containing 11; EC 3.-.-.-; PP1226; WBSCR21
UniProt Protein Function: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: EC 3.-.-.-; HydrolaseChromosomal Location of Human Ortholog: 7q11.23Molecular Function: hydrolase activity
UniProt Protein Details:
NCBI Summary: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. [provided by RefSeq, Mar 2016]
UniProt Code:Q8NFV4
NCBI GenInfo Identifier:74751292
NCBI Gene ID:83451
NCBI Accession:Q8NFV4.1
UniProt Secondary Accession:Q8NFV4,Q6PJU0, Q8N722, Q8N723, Q8NFV2, Q8NFV3, Q9HBS8 H7BYM8
UniProt Related Accession:Q8NFV4
Molecular Weight:28,473 Da
NCBI Full Name:Protein ABHD11
NCBI Synonym Full Names:abhydrolase domain containing 11
NCBI Official Symbol:ABHD11  
NCBI Official Synonym Symbols:PP1226; WBSCR21  
NCBI Protein Information:protein ABHD11
UniProt Protein Name:Protein ABHD11
UniProt Synonym Protein Names:Alpha/beta hydrolase domain-containing protein 11
Protein Family:Protein
UniProt Gene Name:ABHD11  
UniProt Entry Name:ABHDB_HUMAN
Antibodies
ABHD11 Antibody (PACO00355)
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