重组人组蛋白分子伴侣ASF1A报价

特别声明：本产品及我公司所售其他产品均为科研类试剂产品，严禁用于药物、医疗及其他非科研用途。

重组人组蛋白分子伴侣ASF1A报价的品牌：百奥莱博，是优质的分子生物学试剂产品，用于生化研究，本产品质量好，且极具价格优势，深为用户称道，了解更多重组人组蛋白分子伴侣ASF1A等分子生物学试剂产品请联系我司咨询订购。

名称：重组人组蛋白分子伴侣ASF1A报价
英文名：Recombinant Human Histone Chaperone ASF1A
编号：JN0684
规格：10μg|50μg|500μg|1mg
品牌：百奥莱博
产地：国产|进口
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Met204在N端含T7标签，C端含有His标签。

ASF1A质量控制：＞95%(还原性SDS-PAGE)

ASF1A制剂：冻干品

ASF1A保存：
冻干蛋白置于-20℃以下可长期保存，室温条件下可稳定保存3周。
复溶蛋白溶液可在4～7℃保存2～7天，可分装后置于-20℃保存三个月。

ASF1A复溶：
打开试剂管前请先离心。
复溶浓度推荐大于100 μg/ml。
冻干蛋白请溶于ddH2O。
复溶后，请根据用量分装冻存，避免反复冻融。

关于ASF1A：
Human Histone Chaperone ASF1A (ASF1A) belongs to the H3/H4 family of histone chaperone proteins. ASF1A is ubiquitously expressed in many cells and tissues, interacting with histones H3 and H4. ASF1A cooperates with Chromatin Assembly Factor 1 to promote replication-dependent chromatin assembly and with HIRA to promote replication-independent chromatin assembly. In addition, ASF1A is necessary for the formation of senescence-associated heterochromatin foci (SAHF) and efficient senescence-associated cell cycle exit.

重组人组蛋白分子伴侣ASF1A报价极具性价比，此外，我公司正火爆促销以下产品：

·重组人BNIP3
编号：JN0986
英文名称：Recombinant Human Adenovirus E1B 19 kDa Protein-Interacting Protein 3
规格：10μg|50μg|500μg|1mg
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Leu166在N端含有His标签。

BNIP3质量控制：＞95%(还原性SDS-PAGE)

BNIP3制剂：冻干品

BNIP3保存：
冻干蛋白置于-20℃以下可长期保存，室温条件下可稳定保存3周。
复溶蛋白溶液可在4～7℃保存2～7天，可分装后置于-20℃保存三个月。

BNIP3复溶：
打开试剂管前请先离心。
复溶浓度推荐大于100 μg/ml。
冻干蛋白请溶于ddH2O。
复溶后，请根据用量分装冻存，避免反复冻融。

关于BNIP3：
BCL2/Adenovirus E1B 19 kDa Protein-Iinteracting Protein 3 (BNIP3) is a single-pass membrane protein. BNIP3 is a member of the NIP3 family. BNIP3 contains a single Bcl-2 homology 3 domain and interacts with the E1B 19 kDa protein. BNIP3 have been associated with pro-apoptotic function. BNIP3 is an apoptosis-inducing protein that can overcome BCL2 suppression. It plays a role in repartitioning calcium between the two major intracellular calcium stores in association with BCL2. BNIP3 involved in mitochondrial quality control via its interaction with SPATA18/MIEAP, response to mitochondrial damage, participates to mitochondrial protein catabolic process.


重组人组蛋白分子伴侣ASF1A报价关键词：百奥莱博,重组组蛋白分子伴侣ASF1A,重组人组蛋白分子伴侣ASF1A蛋白,Recombinant Human Histone Chaperone ASF1A,JN0684


·重组人牙本质基质蛋白1(DMP-1)
编号：JN0811
英文名称：Recombinant Human Dentin matrix protein 1
规格：10μg|50μg|500μg|1mg
本品由我们的哺乳动物细胞表达系统制备而成，目的基因编码的Lys17-Tyr513在C端含有His标签。

DMP-1质量控制：＞95%(还原性SDS-PAGE)

DMP-1制剂：冻干品

DMP-1保存：
冻干蛋白置于-20℃以下可长期保存，室温条件下可稳定保存3周。
复溶蛋白溶液可在4～7℃保存2～7天，可分装后置于-20℃保存三个月。

DMP-1复溶：
打开试剂管前请先离心。
复溶浓度推荐大于100 μg/ml。
冻干蛋白请溶于ddH2O。
复溶后，请根据用量分装冻存，避免反复冻融。

关于DMP-1：
Dentin Matrix Acidic Phosphoprotein 1 (DMP-1) is an extracellular matrix protein and a member of the small integrin binding ligand N-linked glycoprotein family. DMP-1 is expressed in teeth particularly in odontoblast, ameloblast, and cementoblast. DMP-1 is critical for proper mineralization of bone and dentin. DMP-1 may have a dual function during osteoblast differentiation. In the nucleus of undifferentiated osteoblasts, the unphosphorylated form of DMP-1 acts as a transcriptional component for activation of osteoblast-specific genes like osteocalcin. During the osteoblast to osteocyte transition phase, DMP-1 is phosphorylated and exported into the extracellular matrix, where it regulates nucleation of hydroxyapatite. DMP-1 mutations have also been shown to cause rickets hypophosphatemic autosomal recessive type 1 (ARHR1).


重组人组蛋白分子伴侣ASF1A报价关键词：百奥莱博,重组组蛋白分子伴侣ASF1A,重组人组蛋白分子伴侣ASF1A蛋白,Recombinant Human Histone Chaperone ASF1A,JN0684


·重组人中链酰基辅酶A脱*酶(ACADM)(MCAD)
编号：JN0953
英文名称：Recombinant Human Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
规格：10μg|50μg|500μg|1mg
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Lys26-Asn421在N端含有His标签。

ACADM质量控制：＞95%(还原性SDS-PAGE)

ACADM制剂：液体

ACADM保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于ACADM：
Medium-Chain Specific Acyl-CoA Dehydrogenase (ACADM) is a mitochondrial fatty acid beta-oxidation that belongs to the acyl-CoA dehydrogenase family. ACADM is a homotetramer enzyme that catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. ACADM is specific for acyl chain lengths of 4 to 16. It is essential for converting these particular fatty acids to energy, especially during fasting periods. Defects in ACADM cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death.

我公司正在火爆促销分子生物学试剂系列产品，欢迎您的垂询选购重组人组蛋白分子伴侣ASF1A报价。