Name : Lamin A Antibody
Supplier : NJS POLY
Price :389
SKU : GEN9623022694
| Category | Antibody |
| Concentration | 2ml sterile DI water, 5mg/ml if reconstituted with 0 |
| Form | Antigen affinity purified |
| Conjugation | Unconjugated |
| Clone | Polyclonal antibody |
| Recognised antigen | Lamin A |
| Host animal | Rabbit (Oryctolagus cuniculus) |
| Clonality | Polyclonal (rabbit origin) |
| Species reactivity | Due to limited knowledge and inability to test the antibody against all known species, Mouse (Mus musculus), Rat , we cannot guarantee that no other cross reactivity can occur, Human (Homo sapiens) |
| Tested applications | ICC, IHC-P, WB |
| Recommended dilutions | 5-1ug/ml, 5-1ug/ml, 5-1ug/ml, IHC (Paraffin): 0, Immunocytochemistry: 0, Western blot: 0 |
| Notes | Titration of the Lamin A antibody may be required due to differences in protocols and secondary/substrate sensitivity, The stated application concentrations are suggested starting points |
| Intented use | This Lamin A antibodyis to be used only for research purposes and not for diagnostics |
| Gene ID # | 4000 |
| Purity | Antigen affinity |
| Description | A, Alternative splicing within exon 10 gives rise to two different mRNAs that code for pre-Lamin A and C, Deficiency is thus associated with both defective nuclear mechanics and impaired mechanically activated gene transcription, Lamin A/C is mapped to 1q21, The Lamin A/C (LMNA) gene contains 12 exons, There are three types of lamins, a protein network underlying the inner nuclear membrane that determines nuclear shape and size, and Hutchinson-Gilford progeria syndrome, dilated cardiomyopathy, 2-q21, 3 and mutations in this gene cause a variety of human diseases including Emery-Dreifuss muscular dystrophy, B and C, Lamins are structural protein components of the nuclear lamina |
| Immunogen | Human partial recombinant protein (AA 481-646) was used as the immunogen for this Lamin A antibody |
| Storage | Avoid repeated freezing and thawing, Celcius or lower, Cycles of freezing and thawing can denaturate the peptide chains of the antibodies and reduce their sensitivity and/or change their affinity, For long-term, Prepare aliqotes in such a manner so that freeze-thaw cycles are minimized, aliquot and store at -20 deg, the Lamin A antibody can be stored for up to one month at 4oC, After reconstitution |
| Properties | C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by NJS poly they should be stored frozen at - 24° |
| Gene target | Lamin A |
| Short name | Lamin A Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | Lamin A (Antibody to) |
| Alternative technique | antibodies |
| Identity | 9450 |
| Gene | PRO1 |
| Long gene name | lamin A/C |
| Synonyms gene | LMN1 CMD1A LGMD1B LMNL1 |
| Synonyms gene name | cardiomyopathy, dilated 1A (autosomal dominant) limb girdle muscular dystrophy 1B (autosomal dominant) progeria 1 (Hutchinson-Gilford type) lamin A/C-like 1 |
| Synonyms | HGPS MADA LMNA |
| Synonyms name | mandibuloacral dysplasia type A |
| Locus | 1q22 |
| Discovery year | 1992-04-09 |
| GenBank acession | BC014507 |
| Entrez gene record | 4000 |
| Pubmed identfication | 8511676 8838815 12702809 |
| RefSeq identity | NM_170707 |
| Classification | Lamins |
| Havana BLAST/BLAT | OTTHUMG00000013961 |
| Locus Specific Databases | Inherited Peripheral Neuropathies Mutation Database Leiden Muscular Dystrophy Pages UMD Locus Specific Databases Leiden Muscular Dystrophy pages LRG_254 |