GRIM19 (NDUFA13) (NM_015965) Human Over-expression Lysate

Lysate of GRIM19 over-expression cell lines, WB control

Transient overexpression lysate of NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13 (NDUFA13), nuclear gene encoding mitochondrial protein

Product Info Summary

SKU: LS051079
Size: 100 µg
Expression Host: HEK293T
Tag:

C-Myc/DDK

Description: Transient overexpression lysate of NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13 (NDUFA13), nuclear gene encoding mitochondrial protein

Product Name

GRIM19 (NDUFA13) (NM_015965) Human Over-expression Lysate

See all GRIM19 products

SKU/Catalog Number

LS051079

Size

100 µg

Description

Transient overexpression lysate of NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13 (NDUFA13), nuclear gene encoding mitochondrial protein

Storage & Handling

The lysate is shipped with dry ice. Upon receiving, store the sample at -80°C. Also after dilution, the protein sample should be aliquoted and stored at -80°C for long term storage. Avoid repeated freeze-thaw cycles. Lysate samples can be diluted with 2xSDS Sample Buffer provided. Lysate samples are stable for 12 months from the date of receipt when stored at -80°C.

Cite This Product

GRIM19 (NDUFA13) (NM_015965) Human Over-expression Lysate (Boster Biological Technology, Pleasanton CA, USA, Catalog # LS051079)

Tag

C-Myc/DDK

Detection Antibodies

Clone OTI4C5, Anti-DDK (FLAG) monoclonal antibody (M30971)

Components

1 vial of 100 µg gene specific transient over-expression cell lysate in RIPA buffer

1 vial of 100 µg whole HEK293T cell lysate in RIPA buffer

1 vial of 250ul 2xSDS Sample Buffer (4% SDS, 125mM Tris-HCl pH6.8, 10% Glycerol, 0.002% Bromophenol blue, 100mM DTT)

Preparation

HEK293T cells in 10-cm dishes were transiently transfected with Transfection Reagent and 5ug ORF cDNA plasmid. Transfected cells were cultured for 48hrs before collection. The cells were lysed in modified RIPA buffer (25mM Tris-HCl pH7.6, 150mM NaCl, 1% NP-40, 1mM EDTA, 1xProteinase inhibitor cocktail mix, 1mM PMSF and 1mM Na3VO4), and then centrifuged to clarify the lysate. Protein concentration was measured by BCA kit. Cell lysates were aliquoted and stored at -20°C before shipping.

Validation Images & Assay Conditions

Gene/Protein Information for NDUFA13 (Source: Uniprot.org, NCBI)

Gene Name

NDUFA13

Full Name

NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13

Weight

16.698kDa

Superfamily

complex I NDUFA13 subunit family

Alternative Names

B16.6; CDA016; Cell death regulatory protein GRIM-19; cell death-regulatory protein GRIM19; CI-B16.6; complex I B16.6 subunit; Complex I-B16.6; FLJ58045; FLJ59191; Gene associated with retinoic and IFN-induced mortality 19 protein; Gene associated with retinoic and interferon-induced mortality 19 protein; GRIM-19CGI-39; GRIM19NADH-ubiquinone oxidoreductase B16.6 subunit; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13 NDUFA13 B16.6, CDA016, CGI-39, GRIM-19, GRIM19, MC1DN28 NADH:ubiquinone oxidoreductase subunit A13 NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13|CI-B16.6|NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13|NADH-ubiquinone oxidoreductase B16.6 subunit|cell death regulatory protein GRIM-19|cell death-regulatory protein GRIM19|complex I B16.6 subunit|complex I-B16.6|gene associated with retinoic and IFN-induced mortality 19 protein|gene associated with retinoic and interferon-induced mortality 19 protein

*If product is indicated to react with multiple species, protein information is based on the gene entry specified above in "Species".

For more info on NDUFA13, check out the NDUFA13 Infographic

NDUFA13 infographic

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In this infographic, you will see the following information for NDUFA13: database IDs, superfamily, protein function, synonyms, molecular weight, chromosomal locations, tissues of expression, subcellular locations, post-translational modifications, and related diseases, research areas & pathways. If you want to see more information included, or would like to contribute to it and be acknowledged, please contact us [email protected].

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