ERAB (HSD17B10) (NM_004493) Human Over-expression Lysate

Lysate of ERAB over-expression cell lines, WB control

Transient overexpression lysate of hydroxysteroid (17-beta) dehydrogenase 10 (HSD17B10), nuclear gene encoding mitochondrial protein, transcript variant 1

Product Info Summary

SKU: LS003028
Size: 100 µg
Expression Host: HEK293T
Tag:

C-Myc/DDK

Description: Transient overexpression lysate of hydroxysteroid (17-beta) dehydrogenase 10 (HSD17B10), nuclear gene encoding mitochondrial protein, transcript variant 1

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Product Name

ERAB (HSD17B10) (NM_004493) Human Over-expression Lysate

See all ERAB products

SKU/Catalog Number

LS003028

Size

100 µg

Description

Transient overexpression lysate of hydroxysteroid (17-beta) dehydrogenase 10 (HSD17B10), nuclear gene encoding mitochondrial protein, transcript variant 1

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

ERAB (HSD17B10) (NM_004493) Human Over-expression Lysate (Boster Biological Technology, Pleasanton CA, USA, Catalog # LS003028)

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 HSD17B10 (Source: Uniprot.org, NCBI)

Gene Name

HSD17B10

Full Name

3-hydroxyacyl-CoA dehydrogenase type-2

Weight

26.923kDa

Superfamily

short-chain dehydrogenases/reductases (SDR) family

Alternative Names

17-beta-HSD 10; 17-beta-hydroxysteroid dehydrogenase 10; 17b-HSD10; 3-hydroxy-2-methylbutyryl-CoA dehydrogenase; ABAD; amyloid-beta peptide binding alcohol dehydrogenase; CAMR; DUPXp11.22; EC 1.1.1.178; EC 1.1.1.35; Endoplasmic reticulum-associated amyloid beta-peptide-binding protein; ERAB3-hydroxyacyl-CoA dehydrogenase type-2; HADH2AB-binding alcohol dehydrogenase; hydroxyacyl-Coenzyme A dehydrogenase, type II, hydroxyacyl-Coenzyme Adehydrogenase, type II; hydroxysteroid (17-beta) dehydrogenase 10; mental retardation, X-linked, syndromic 10; MHBD; Mitochondrial ribonuclease P protein 2,3-hyd HSD17B10 17b-HSD10, ABAD, CAMR, DUPXp11.22, ERAB, HADH2, HCD2, HSD10MD, MHBD, MRPP2, MRX17, MRX31, MRXS10, SCHAD, SDR5C1 hydroxysteroid 17-beta dehydrogenase 10 3-hydroxyacyl-CoA dehydrogenase type-2|3-hydroxy-2-methylbutyryl-CoA dehydrogenase|AB-binding alcohol dehydrogenase|amyloid-beta peptide binding alcohol dehydrogenase|endoplasmic reticulum-associated amyloid beta-peptide-binding protein|mitochondrial RNase P subunit 2|mitochondrial ribonuclease P protein 2|short chain L-3-hydroxyacyl-CoA dehydrogenase type 2|short chain type dehydrogenase/reductase XH98G2

*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 HSD17B10, check out the HSD17B10 Infographic

HSD17B10 infographic

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In this infographic, you will see the following information for HSD17B10: 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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