Name : lamin A/C Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN8452475922
| Long name | lamin A/C Primary Polyclonal Antibody |
| Also known as | lamin A/C PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | lamin A/C |
| Specificity | This is a highly specific antibody against lamin A/C |
| Modification(s) | None |
| Modification site(s) | Unmodified antibody |
| Clonality | Polyclonal antibody |
| Clone number | Polyclonal antibody |
| Concentration | 1ug per 1ul |
| Subcellular location | Nucleus |
| Source | This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human lamin A |
| Gene ID number | 4000 |
| Swiss Prot | P02545 |
| Tested Applications | IF(ICC), IF(IHC-P), IHC-P, WB |
| Recommended dilutions | IF(ICC)(1:50-200), IF(IHC-P)(1:50-200), IHC-P(1:100-500), WB(1:100-1000) |
| Cross reactivity | Mouse, Rat, Human |
| Cross reactive species details | not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Background of the target antigen | Also prevents fat infiltration of muscle and bone marrow, It acts to disrupt mitosis and induce DNA damage in vascular smooth muscle cells (VSMCs), Lamin A and C are present in equal amounts in the lamina of mammals, Plays an important role in nuclear assembly, Prelamin-A/C can accelerate smooth muscle cell senescence, Required for normal development of peripheral nervous system and skeletal muscle and for muscle satellite cell proliferation, Required for osteoblastogenesis and bone formation, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, and premature senescence, chromatin organization, genomic instability, helping to maintain the volume and strength of skeletal muscle and bone, leading to mitotic failure, nuclear membrane and telomere dynamics, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin, Lamins are components of the nuclear lamina |
| Purification method | This antibody was purified via Protein A |
| Storage conditions | 50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA |
| Synonym names | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNA, LMNC, LMNL1, PRO1, Prelamin-A/C, FPL |
| Properties | C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24° |
| Gene target | lamin A/C |
| Short name | lamin A/C Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | lamin A/C (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 |