- Antibody type:Primary
- Antigen name:HSP22
- Clonality:Polyclonal
- Conjugation:Alexa Fluor® 680
- Host:Rabbit
- ImmunoChemistry:Yes
- ImmunoFluorescence:Yes
- Isotype:IgG
- Reactivity:Human,Mouse
- Western blot:Yes
- Epitope:101-196/196
- Form:Liquid
- Gene ID:26353
- Antigen synonyms:DHMN2|E2IG1|HSPB8|Heat shock 22kDa protein 8|Spinal muscular atrophy distal adult autosomal dominant|Small stress protein like protein HSP22|Charcot Marie Tooth disease axonal type 2L|Hereditary motor neuropathy distal|HSPB 8|E2 induced gene 1 protein|Heat shock protein 22|Protein kinase H11|Alpha crystallin C chain|Charcot Marie Tooth disease spinal|HMN2|DHMN 2|H11|HMN 2|CRYAC|Heat shock protein beta 8|CMT2L|HSB8
- Modification:Unmodified
- Storage buffer:Aqueous buffered solution containing 0,01 M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol
- Molecular weight:22 kDa
- Storage temperature:Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Concentration:1 µg/µl
- Shipping temperature:4 °C
- Immunogen:KLH conjugated synthetic peptide derived from human HSP22
- Tested applications:ICC
- Purification:Purified by Protein A
- Pack type:Vial
- Pk:100 µl
Hsp22 (HSPB8) is a 196-amino acid protein that contains a central portion homologous to a highly conserved HSP-alpha crystallin domain common to all the small heat shock protein (HSP20) family members. Hsp22 is a monomeric protein which interacts with HSPB1. It displays temperature-dependent chaperone activity. The highest abundance of Hsp22 is in skeletal muscle, heart, and placenta. Mutations in the HSPB8 gene are associated with the inherited peripheral neuropathies, autosomal dominant distal hereditary motor neuropathy type IIA (dSMA) and axonal Charcot-Marie-Tooth disease type 2L (CMT2L).
Type: Primary
Antigen: HSP22
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 680
Public Immunogen Range: 101-196/196
Host: Rabbit
Isotype: IgG
Reactivity: Human; Mouse; Others