HMGCL anticorps (N-Term)
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- Antigène Voir toutes HMGCL Anticorps
- HMGCL (3-Hydroxymethyl-3-Methylglutaryl-CoA Lyase (HMGCL))
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Épitope
- AA 71-99, N-Term
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp HMGCL est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This HMGCL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-99 amino acids from the N-terminal region of human HMGCL.
- Clone
- RB22965
- Isotype
- Ig Fraction
- Top Product
- Discover our top product HMGCL Anticorps primaire
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- Indications d'application
- WB: 1:1000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- HMGCL Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
- Date de péremption
- 6 months
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- Antigène
- HMGCL (3-Hydroxymethyl-3-Methylglutaryl-CoA Lyase (HMGCL))
- Autre désignation
- HMGCL (HMGCL Produits)
- Synonymes
- anticorps Afu7g01720, anticorps AO090038000541, anticorps AW476067, anticorps HL, anticorps zgc:56248, anticorps 3-hydroxymethyl-3-methylglutaryl-CoA lyase S homeolog, anticorps 3-hydroxymethyl-3-methylglutaryl-CoA lyase, anticorps 3-hydroxymethyl-3-methylglutaryl-Coenzyme A lyase, anticorps 3-hydroxy-3-methylglutaryl-Coenzyme A lyase, anticorps hmgcl.S, anticorps HMGCL, anticorps AFUA_7G01720, anticorps NFIA_114450, anticorps ACLA_065820, anticorps AOR_1_910074, anticorps PMAA_004600, anticorps TSTA_103060, anticorps ARB_04874, anticorps TRV_06573, anticorps Hmgcl, anticorps hmgcl
- Sujet
- The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].
- Poids moléculaire
- 34360
- ID gène
- 3155
- NCBI Accession
- NP_000182, NP_001159531
- UniProt
- P35914
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