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PTCD1 Polyclonal antibody, PBS Only

PTCD1 Polyclonal Antibody for WB, Indirect ELISA

Cat No. 33057-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, Indirect ELISA

KIAA0632, Pentatricopeptide repeat-containing protein 1, mitochondrial

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

33057-1-PBS targets PTCD1 in WB, Indirect ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag37639

Product name: Recombinant human PTCD1 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 201-595 aa of BC003688

Sequence: VWRLMLSLGLQPSRDSYNLLLVAARDCGLGDPQVASELLLKPREEATVLQPPVSRQRPRRTAQAKAGNLMSAMLHVEALERQLFLEPSQALGPPEPPEARVPGKAQPEVDTKAEPSHTAALTAVALKPPPVELEVNLLTPGAVPPTVVSFGTVTTPADRLALIGGLEGFLSKMAEHRQQPDIRTLTLLAEVVESGSPAESLLLALLDEHQVEADLTFFNTLVRKKSKLGDLEGAKALLPVLAKRGLVPNLQTFCNLAIGCHRPKDGLQLLTDMKKSQVTPNTHIYSALINAAIRKLNYTYLISILKDMKQNRVPVNEVVIRQLEFAAQYPPTFDRYQGKNTYLEKIDGFRAYYKQWLTVMPAEETPHPWQKFRTKPQGDQDTGKEADDGCALGGR

Predict reactive species
Full Name pentatricopeptide repeat domain 1
Calculated Molecular Weight 79 kDa
Observed Molecular Weight72 kDa
GenBank Accession NumberBC003688
Gene Symbol PTCD1
Gene ID (NCBI) 26024
RRIDAB_3742841
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity Purification
UNIPROT IDO75127
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

PTCD1 protein (Pentatricopeptide Repeat Domain 1) is a nuclear gene-encoded protein located in the mitochondrial matrix. Its core function lies in regulating mitochondrial gene expression and the assembly of the respiratory chain. It specifically recognizes and binds to mitochondrial RNA (such as mRNA or pre-RNA) through its characteristic pentapeptide repeat sequence (PPR) motif, participating in RNA processing, stability maintenance, or translation processes, thereby being crucial for the assembly and function of mitochondrial oxidative phosphorylation complexes (especially complex I). Its deficiency is associated with mitochondrial dysfunction, neurodegenerative diseases, and cardiomyopathy and other pathological processes.

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