TAF1B (NM_005680) Human Recombinant Protein

CAT#: TP762071

Purified recombinant protein of Human TATA box binding protein (TBP)-associated factor, RNA polymerase I, B, 63kDa (TAF1B),Met1-Lys208, with N-terminal His tag, expressed in E. coli, 50ug



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CNY 2,050.00


货期*
2周

规格
    • 50 ug

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经常一起买 (1)
TAF1B mouse monoclonal antibody, clone OTI1A8 (formerly 1A8)
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Species Human
Expression Host E. coli
Expression cDNA Clone or AA Sequence
A DNA sequence encoding the region(Met1-Lys208) of TAF1B
Tag N-His
Predicted MW 23.7 kDa
Concentration >0.05 µg/µL as determined by microplate BCA method
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Buffer 50 mM Tris-HCl, pH 8.0, 8 M urea
Note For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process.
Storage Store at -80°C.
Stability Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
Reference Data
RefSeq NP_005671
Locus ID 9014
UniProt ID Q53T94
Refseq Size 2306
Cytogenetics 2p25.1
Refseq ORF 1764
Synonyms MGC:9349; RAF1B; RAFI63; SL1; TAFI63
Summary Initiation of transcription by RNA polymerase I requires the formation of a complex composed of the TATA-binding protein (TBP) and three TBP-associated factors (TAFs) specific for RNA polymerase I. This complex, known as SL1, binds to the core promoter of ribosomal RNA genes to position the polymerase properly and acts as a channel for regulatory signals. This gene encodes one of the SL1-specific TAFs. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Protein Families Transcription Factors
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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