Donkey anti Human Lambda light chain
英文名称: Donkey anti Human Lambda light chain
型号:null    抗体货号: 500-M324
价格:请致电:010-57128832,18610462672
品牌: 美国/中国    产品商标: fitzgerald

上海信裕生物科技有限公司是一家集研发、生产、销售、服务于一体的国际领先生物高新技术企业,专营基因、蛋白、抗体、Elisa试剂盒、细胞生物学,分子生物学等高质量生物产品。抗体纯化/标记/免疫检测:免疫分析检测是一项应用广泛的技术,利用抗原和抗体的特异性反应进行检测的一种手段,广泛用于医学病理学、免疫组织化学、分子生物学、生物制药等领域的分析研究与技术测定。制备高特异性、高效价的抗体是实验免疫学技术的基础,抗体质量的高低将直接影响试验的成败。抗体纯化能降低非特异性本底,抗体标记能通过标记物的增强放大效应提高检测灵敏度,采用ELISA、WB、IP、IHC等不同免疫分析技术检测各种样品中特定的目的蛋白。 

ed in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Lamin B2,核纤层蛋白B2抗体PubMedPubMed
产品介绍background:
A unique family of Cysteine proteases has been described that differs in sequence, structure and substrate specificity from any previously described protease family. This family, termed CED-3/ICE, functions as key components of the apoptotic machinery and act to destroy specific target proteins which are critical to cellular longevity. Nuclear lamins are critical to maintaining the integrity of the nuclear envelope and cellular morphology as components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin. B-type lamins undergo a series of modifications, such as farnesylation and phosphorylation. Increased phosphorylation of the lamins occurs before envelope disintegration and probably plays a role in regulating lamin associations. Nuclear Lamin B is fragmented as a consequence of apoptosis by an unidentified member of the ICE family.

Function:
Lamins are components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin.

Subunit:
Interacts with TMEM43 (By similarity).

Subcellular Location:
Nucleus inner membrane; Lipid-anchor; Nucleoplasmic side.

Post-translational modifications:
B-type lamins undergo a series of modifications, such as farnesylation and phosphorylation. Increased phosphorylation of the lamins occurs before envelope disintegration and probably plays a role in regulating lamin associations.

DISEASE:
Defects in LMNB2 are a cause of partial acquired lipodystrophy (APLD) [MIM:608709]. A rare childhood disease characterized by loss of subcutaneous fat from the face and trunk. Fat deposition on the pelvic girdle and lower limbs is normal or excessive. Most frequently, onset between 5 and 15 years of age. Most affected subjects are females and some show no other abnormality, but many develop glomerulonephritis, diabetes mellitus, hyperlipidemia, and complement deficiency. Mental retardation in some cases. APLD is a sporadic disorder of unknown etiology.

Similarity:
Belongs to the intermediate filament family.

Database links:
Entrez Gene: 84823 Human
Entrez Gene: 16907 Mouse
Entrez Gene: 299625 Rat
Omim: 150341 Human
SwissProt: Q03252 Human
SwissProt: P21619 Mouse
Unigene: 728836 Human
Unigene: 7362 Mouse

Lamin B2,核纤层蛋白B2抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

t 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
Tissue/cell: mouse embryo tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; 
Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; 
Incubation: Anti-PTPRD Polyclonal Antibody, Unconjugated(HZ-11471R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining