抗体

山羊抗DYNC1H1抗体

MBS422138

0.1毫克

225美元

多克隆

山羊

未共轭

人类, 大鼠

酶联免疫吸附测定, 酶免疫法

抗体

山羊抗DYNC1H1抗体

DYNC1H1

DYNC1H1; dynein, cytoplasmic 1, heavy chain 1; DHC1; DHC1a; DKFZp686P2245; DNCH1; DNCL; DNECL; DYHC; Dnchc1; HL-3; KIAA0325; p22; DYNC1H1 variant protein; cytoplasmic dynein heavy chain; dynein heavy chain, cytosolic; dynein, cytoplasmic, heavy polypeptid; DYNC1H1 antibody; dynein; cytoplasmic 1; heavy chain 1 antibody; DHC1 antibody; DHC1a antibody; DKFZp686P2245 antibody; DNCH1 antibody; DNCL antibody; DNECL antibody; DYHC antibody; Dnchc1 antibody; HL-3 antibody; KIAA0325 antibody; p22 antibody; DYNC1H1 variant protein antibody; cytoplasmic dynein heavy chain antibody; dynein heavy chain; cytosolic antibody; dynein; cytoplasmic; heavy polypeptide 1 antibody; dynein; cytoplasmic-like antibody

cytoplasmic dynein 1 heavy chain 1; Cytoplasmic dynein 1 heavy chain 1; cytoplasmic dynein 1 heavy chain 1; dynein cytoplasmic 1 heavy chain 1; Cytoplasmic dynein heavy chain 1; Dynein heavy chain, cytosolic

DYNC1H1

DYNC1H1;DYNC1H1;p22;DHC1;DNCL;DYHC;HL-3;CMT2O;DHC1a;DNCH1;DNECL;Dnchc1;SMALED1;DHC1;DNCH1;DNCL;DNECL;DYHC;KIAA0325

DYHC1_HUMAN

多克隆

山羊

Expected from sequence similarity: Human, Rat

4646

EKKTRTDSTSDGRP

通过硫酸铵沉淀和用免疫多肽抗原亲和层析从山羊血清中纯化得到的

Supplied at 0.5 mg/ml in Tris saline, 0. 02% sodium azide, pH7.3 with 0.5% bovine serum albumin.

100ug specific antibody in 200ul

Aliquot and store at -20 degree C. Minimize freezing and thawing.

肽酶联免疫吸附测定(EIA)

Peptide ELISA: Antibody detection limit dilution 1: 4000. Western Blot: Not yet tested - our routinely used western blotting protocol does not allow detection of proteins as large as the calculated size of 532kDa according to NP_001367.2. Therefore we cannot recommend an optimal concentration and the antibody is an aspiring product.

Immunogen: Peptide with sequence C-EKKTRTDSTSDGRP, from the internal region of the protein sequence according to NP_001367.2. Epitope: Internal region

33350932

NP_001367.2

NM_001376.4

532,408 Da

AURKA Activation By TPX2 Pathway (1383018); Adaptive Immune System Pathway (1269171); Anchoring Of The Basal Body To The Plasma Membrane Pathway (1268847); Asparagine N-linked Glycosylation Pathway (1268714); Assembly Of The Primary Cilium Pathway (1268846); COPI-independent Golgi-to-ER Retrograde Traffic Pathway (1383043); COPI-mediated Anterograde Transport Pathway (1339109); Cell Cycle Pathway (1269741); Cell Cycle, Mitotic Pathway (1269763); Centrosome Maturation Pathway (1269805)

Dyneins are a group of microtubule-activated ATPases that function as molecular motors. They are divided into two subgroups of axonemal and cytoplasmic dyneins. The cytoplasmic dyneins function in intracellular motility, including retrograde axonal transport, protein sorting, organelle movement, and spindle dynamics. Molecules of conventional cytoplasmic dynein are comprised of 2 heavy chain polypeptides and a number of intermediate and light chains.This gene encodes a member of the cytoplasmic dynein heavy chain family. [provided by RefSeq, Oct 2008]

DNCH1: Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Defects in DYNC1H1 are the cause of Charcot-Marie-Tooth disease type 2O (CMT2O). CMT2O is anaxonal form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies (designated CMT1 when they are dominantly inherited) and primary peripheral axonal neuropathies (CMT2). Neuropathies of the CMT2 group are characterized by signs of axonal degeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy. Nerve conduction velocities are normal or slightly reduced. Defects in DYNC1H1 are the cause of mental retardation autosomal dominant type 13 (MRD13). A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. MRD13 is associated with variable neuronal migration defects and mild dysmorphic features. Some patients may also show signs of peripheral neuropathy, such as abnormal gait and hyporeflexia. Defects in DYNC1H1 are the cause of spinal muscular atrophy, lower extremity, autosomal dominant (SMALED). A form of spinal muscular atrophy, a neuromuscular disorder characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy. SMALED is characterized by muscle weakness predominantly affecting the proximal lower extremities. Belongs to the dynein heavy chain family. Protein type: Motility/polarity/chemotaxis; Motor; Microtubule-binding. Chromosomal Location of Human Ortholog: 14q32. Cellular Component: centrosome; cytoplasmic dynein complex; cytosol; filopodium; membrane; microtubule. Molecular Function: ATP binding; ATPase activity; dynein light intermediate chain binding; microtubule motor activity; protein binding. Biological Process: antigen processing and presentation of exogenous peptide antigen via MHC class II; cytoplasmic mRNA processing body assembly; ER to Golgi vesicle-mediated transport; establishment of spindle localization; G2/M transition of mitotic cell cycle; metabolic process; microtubule-based movement; mitotic spindle organization and biogenesis; stress granule assembly. Disease: Charcot-marie-tooth Disease, Axonal, Type 2o; Mental Retardation, Autosomal Dominant 13; Spinal Muscular Atrophy, Lower Extremity-predominant, 1, Autosomal Dominant

0.1毫克

225美元