Recombinant; Rabbit anti Human Reelin Antibody; WB; Unconjugated
| SKU | Size | Availability | Price | Qty |
|---|---|---|---|---|
| Ab124937-10μl | 10μl | In stock | $79.90 | |
| Ab124937-50μl | 50μl | In stock | $239.90 | |
| Ab124937-100μl | 100μl | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $409.90 | |
| Ab124937-1ml | 1ml | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $3,299.90 |
Recombinant; Rabbit anti Human Reelin Antibody; WB; Unconjugated
| Product Name | Recombinant Reelin Antibody - Primary antibody, specific to Reelin, Rabbit IgG |
|---|---|
| Synonyms | ETL7; LIS2; PRO1598; EC 3.4.21; EC 3.4.21.-; Reeler; Reelin; RELN; RL; RLPRO1598; LIS2 antibody; PRO1598 antibody; Reeler antibody; Reelin antibody; RELN antibody; RELN_HUMAN antibody; RL antibody |
| Specifications & Purity | ExactAb™, Validated, Recombinant, 1.1 mg/mL |
| Host species | Rabbit |
| Specificity | Reelin |
| Immunogen | A synthetic peptide derived from human Reelin (AA 3240-3300). |
| Positive Control | WB: Hep G2 and C6 cell lysates. |
| Conjugation | Unconjugated |
| Grade | ExactAb™, Recombinant, Validated |
| Product Description |
Rabbit anti Human Reelin Antibody, Recombinant, could be used for WB and so on. |
| Isotype | Rabbit IgG |
|---|---|
| Light Chain Type | kappa |
| SDS-PAGE | 150 kDa |
| Purification Method | Protein A purified |
| Form | Liquid |
| Concentration | 1.1 mg/mL |
| Storage Temp | Store at -20°C,Avoid repeated freezing and thawing |
| Shipped In | Ice chest + Ice pads |
| Stability And Storage | Store at 4°C short term (1-2 weeks). Store at -20°C long term (24 months). Upon delivery aliquot. Avoid freeze/thaw cycle. |
Recombinant Reelin Antibody (Ab124937) - Western Blot
All lanes: Recombinant Reelin Antibody (Ab124937) at 1/2000 dilution
Samples: Lysates at 20 µg per lane
Secondary: Goat Anti-Rabbit IgG H&L (HRP) (Ab170144) at 1/20000 dilution
Predicted band size: 388 kDa
Observed band size: 100, 388 kDa
Exposure time: 100.0 s
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Application | Dilution info |
|---|---|
| WB | 1/500-1/2000 |
Enter Lot Number to search for COA:
To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 ZJ24F0404690 | Certificate of Analysis | Apr 19, 2024 | Ab124937 |
| ZJ24F0404689 | Certificate of Analysis | Apr 19, 2024 | Ab124937 |
| 1. Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R et al.. (2003) Human chromosome 7: DNA sequence and biology.. Science, 300 (5620): (767-72). [PMID:12690205] |
| 2. DeSilva, U U and 6 more authors.. (1997) The human reelin gene: isolation, sequencing, and mapping on chromosome 7.. Genome research, [PMID:9049633] |
| 3. Impagnatiello, F F and 13 more authors.. (1998) A decrease of reelin expression as a putative vulnerability factor in schizophrenia.. Proceedings of the National Academy of Sciences of the United States of America, (22): [PMID:9861036] |
| 4. Lambert de Rouvroit, C C, Bernier, B B, Royaux, I I, de Bergeyck, V V and Goffinet, A M AM.. (1999) Evolutionarily conserved, alternative splicing of reelin during brain development.. Experimental neurology, [PMID:10328932] |
| 5. Hong, S E SE and 7 more authors.. (2000) Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.. Nature genetics, [PMID:10973257] |
| 6. Persico, A M AM and 22 more authors.. (2001) Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.. Molecular psychiatry, [PMID:11317216] |
| 7. Hillier, Ladeana W LW and 106 more authors.. (2003) The DNA sequence of human chromosome 7.. Nature, (10): [PMID:12853948] |
| 8. Dazzo, Emanuela E and 22 more authors.. (2015) Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.. American journal of human genetics, (4): [PMID:26046367] |
