p62/SQSTM1 Lysate (NBL1-16446)

p62/SQSTM1 Lysate

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p62/SQSTM1 Lysate Summary:
Applications:WB
Gene:SQSTM1
Purity:Protein
Specificity:Homo sapiens sequestosome 1 (SQSTM1), transcript variant 2, mRNA.
 
Note: Not all species have been tested for usefulness with this product. Only those species listed have been tested. We cannot make any guarantees about additional reactivities which may or may not occur.
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p62/SQSTM1 Lysate Details:
Immunogen:The lysate was created in HEK293T cells, using plasmid ID RC203214 and based on accession number NM_003900. The protein contains a C-terminal DDK tag.
Lysate Details:
Type: OverexpressionLife Stage: Adult
Protein State: Native Tissue Condition: Normal
Sub-cellular Fraction: Whole
Applications:
Uses:This product is intended for use as a positive control in Western Blot. You will receive the lysate (100ug), and an empty vector negative control (100 ug).
Dilutions:Western Blot
TMW:47.5 kDa
Unit Size:0.1 mg
Concentration:1.0 mg/ml
Notes:
This product is manufactured by and sold under license from OriGene Technologies and its use is limited solely for research purposes. Please note that “1 mg/ml” refers to the total protein concentration and that the specific protein concentration is not determined at this time.
Packaging:
Storage:Store at -80 °C. Avoid freeze-thaw cycles.
Buffer:RIPA buffer
Limitations:This product is for research use only and is not approved for use in humans or in clinical diagnosis. Products are guaranteed for 6 months from date of receipt, except for peptides and proteins which are guaranteed for 3 months.
Gene Symbol: SQSTM1
Entrez8878 (Human)
Swiss ProtNM_003900 (Human)
 
Background:

This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq]. Transcript Variant: This variant (2) differs in the 5' UTR, compared to variant 1. Variant 1, 2, and 3 encode the same protein. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

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p62/SQSTM1 Lysate Images (1)
Western Blot: SQSTM1 Lysate [NBL1-16446] - Western Blot experiments. Left-Control; Right -Over-expression Lysate for SQSTM1
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Jump to: Lysates, Peptides and Proteins, Primary Antibodies, RNAi

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