HSPD1 Antikörper (C-Term)
Kurzübersicht für HSPD1 Antikörper (C-Term) (ABIN2792215)
Target
Alle HSPD1 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- C-Term
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Sequenz
- PTKVVRTALL DAAGVASLLT TAEVVVTEIP KEEKDPGMGA MGGMGGGMGG
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Homologie
- Guinea Pig: 90%, Human: 84%, Rabbit: 84%, Rat: 84%
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Produktmerkmale
- This is a rabbit polyclonal antibody against HSPD1. It was validated on Western Blot using a cell lysate as a positive control.
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Aufreinigung
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human HSPD1
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Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
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Kommentare
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Antigen size: 573 AA
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- Avoid repeated freeze-thaw cycles.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- HSPD1 (Heat Shock 60kDa Protein 1 (Chaperonin) (HSPD1))
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Andere Bezeichnung
- HSPD1
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Hintergrund
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HSPD1 is a member of the chaperonin family. This mitochondrial protein may function as a signaling molecule in the innate immune system. It is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Two pseudogenes, both located on chromosome 8, have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.
Alias Symbols: CPN60, GROEL, HSP60, HSP65, HuCHA60, SPG13, HLD4, HSP-60
Protein Interaction Partner: RGS20, NOTCH2NL, KRTAP10-3, KRTAP10-8, SAMD3, KRT40, LZTS2, CEP70, HUWE1, TMCC2, KRT31, KRTAP5-9, FUS, TUBGCP3, AURKB, VCP, UBC, TUBG1, AURKA, SUMO3, LGALS3BP, CDC20, STAU1, LGR4, NEDD8, MDM2, ERG, ASB4, EED, MAPK14, ATP6V1A, RAB1B, C12orf10, NAGK, C11orf
Protein Size: 573 -
Molekulargewicht
- 61 kDa
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Gen-ID
- 3329
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NCBI Accession
- NM_002156, NP_002147
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UniProt
- P10809
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Pathways
- Activation of Innate immune Response, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity
Target
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