ABHD11 Antibody (PACO22109)
- SKU:
- PACO22109
- Product Type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- ELISA
- Applications:
- WB
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Description
| 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 |
 | Western 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) |
| Secondary Antibody |
| Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014) |
| Recommended Products |
| Anti-FITC Goat Anti-Rabbit IgG (H+L) Antibody (CABS011) |
| Anti-HRP-conjugated Beta Actin Antibody (CABC028) |
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