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Rabbit Anti-HSPB8 Antibody (CSB-PA891531ESR2HU)
Supplier: CUSABIO BIOTECH CO.
HspB8 Antibody,Alpha-crystallin C chain Antibody,E2-induced gene 1 protein Antibody,Protein kinase H11 Antibody,Small stress protein-like protein HSP22 Antibody,HSPB8 Antibody,CRYAC Antibody, E2IG1 Antibody, HSP22 Antibody,PP1629 AntibodyMore alternative names for the antibody
Alpha crystallin C chain antibody|Alpha-crystallin C chain antibody|Charcot Marie Tooth disease axonal type 2L antibody|Charcot Marie Tooth disease spinal antibody|CMT2L antibody|CRYAC antibody|DHMN 2 antibody|DHMN2 antibody|E2 induced gene 1 protein antibody|E2-induced gene 1 protein antibody|E2IG1 antibody|H11 antibody|Heat shock 22kDa protein 8 antibody|Heat shock 27kDa protein 8 antibody|Heat shock protein 22 antibody|Heat shock protein beta 8 antibody|Heat shock protein beta-8 antibody|Hereditary motor neuropathy distal antibody|HMN 2 antibody|HMN2 antibody|HMN2A antibody|HSB8 antibody|HSPB 8 antibody|HspB8 antibody|HSPB8_HUMAN antibody|OTTHUMP00000239768 antibody|Protein kinase H11 antibody|Small stress protein like protein HSP22 antibody|Small stress protein-like protein HSP22 antibody|Spinal muscular atrophy distal adult autosomal dominant antibody
Anti-Hsp22 antibody [EPR9714] (ab151552)
Anti-Hsp22 antibody [EPR9714] (ab151552)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Heat shock protein beta-8 protein (1-196AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=26353" target="_blank">Entrez Gene:26353( Human)</a>, <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=80888" target="_blank">Entrez Gene:80888( Mouse)</a>, <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=113906" target="_blank">Entrez Gene:113906( Rat)</a>, <a href="http://www.ncbi.nlm.nih.gov/omim/608014" target="_blank">Omim:608014( Human)</a>, <a href="http://www.uniprot.org/uniprot/Q9UJY1" target="_blank">SwissProt:Q9UJY1( Human)</a>, <a href="http://www.uniprot.org/uniprot/Q9JK92" target="_blank">SwissProt:Q9JK92( Mouse)</a>, <a href="http://www.uniprot.org/uniprot/Q9EPX0" target="_blank">SwissProt:Q9EPX0( Rat)</a>, <a href="http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=400095" target="_blank">Unigene:400095( Human)</a>, <a href="http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=21549" target="_blank">Unigene:21549( Mouse)</a>, <a href="http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=102906" target="_blank">Unigene:102906( Rat)</a>
|Protein function|| |
Displays temperature-dependent chaperone activity.
|Protein tissue specificity|| |
Predominantly expressed in skeletal muscle and heart. .
|Involvement in disease|| |
Neuronopathy, distal hereditary motor, 2A (HMN2A) [MIM:158590]: A neuromuscular disorder. Distal hereditary motor neuronopathies constitute a heterogeneous group of neuromuscular disorders caused by selective degeneration of motor neurons in the anterior horn of the spinal cord, without sensory deficit in the posterior horn. The overall clinical picture consists of a classical distal muscular atrophy syndrome in the legs without clinical sensory loss. The disease starts with weakness and wasting of distal muscles of the anterior tibial and peroneal compartments of the legs. Later on, weakness and atrophy may expand to the proximal muscles of the lower limbs and/or to the distal upper limbs. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Charcot-Marie-Tooth disease 2L (CMT2L) [MIM:608673]: An axonal 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. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the small heat shock protein (HSP20) family.
|Protein cellular localization|| |
Cytoplasm . Nucleus . Note=Translocates to nuclear foci during heat shock.
|Research area|| |
<a href="https://antibodyplus.com/research-areas/">All research areas</a>><a href="https://antibodyplus.com/Signaling-Intermediates/">Signaling Intermediates</a>><a href="https://antibodyplus.com/product-tag/Crystallin/">Crystallin</a><br><a href="https://antibodyplus.com/product-tag/Signaling-Intermediates/"> (View all antibody categories related to Signaling Intermediates)</a>
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CUSABIO BIOTECH CO.
|Product type|| |
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