DNAJC19 antibody (AA 1-116)

Catalog No. ABIN6139722

Product Details anti-DNAJC19 Antibody

Target: DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))

Binding Specificity: AA 1-116

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DNAJC19 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Sequence: MASTVVAVGL TIAAAGFAGR YVLQAMKHME PQVKQVFQSL PKSAFSGGYY RGGFEPKMTK REAALILGVS PTANKGKIRD AHRRIMLLNH PDKGGSPYIA AKINEAKDLL EGQAKK

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-116 of human DNAJC19 (NP_660304.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:200

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for DNAJC19

Target: DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))

Alternative Name: DNAJC19 (DNAJC19 Products)

Synonyms: PAM18 antibody, TIM14 antibody, TIMM14 antibody, 1810055D05Rik antibody, AA959924 antibody, Tim14 antibody, zgc:73251 antibody, DNAJC19 antibody, DKFZp469M2132 antibody, Gm15118 antibody, RGD1560220 antibody, DnaJ heat shock protein family (Hsp40) member C19 antibody, DnaJ (Hsp40) homolog, subfamily C, member 19 antibody, DnaJ heat shock protein family (Hsp40) member C19 L homeolog antibody, Pam18p antibody, DnaJ heat shock protein family (Hsp40) member C19, pseudogene antibody, DNAJC19 antibody, Dnajc19 antibody, dnajc19 antibody, dnajc19.L antibody, PAM18 antibody, Dnajc19-ps antibody

Background: The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19.,DNAJC19,PAM18,TIM14,TIMM14,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Neuroscience,DNAJC19

Molecular Weight: 10 kDa/12 kDa

Gene ID: 131118

UniProt: Q96DA6

Pathways: SARS-CoV-2 Protein Interactome