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SAB1404142

Sigma-Aldrich

Monoclonal Anti-NPAS2 antibody produced in mouse

clone 6C9, ascites fluid

Synonym(s):

FLJ23138, MGC71151, MOP4, PASD4, bHLHe9

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

Pricing and availability is not currently available.

biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

6C9, monoclonal

mol wt

antigen ~36.34 kDa

species reactivity

human

technique(s)

indirect ELISA: suitable
western blot: 1-5 μg/mL

isotype

IgG2aκ

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This Item
D6319PLA0262WH0083594M1
antibody form

serum

antibody form

affinity isolated antibody

antibody form

affinity purified immunoglobulin

antibody form

purified immunoglobulin

biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

mouse

species reactivity

mouse, human

species reactivity

rat, mouse, human

species reactivity

human

species reactivity

human

Gene Information

human ... DCP2(167227)

Gene Information

human ... DCP2(167227)
mouse ... Dcp2(20640)
rat ... Dcp2(291604)

Gene Information

rabbit ... Dcp2(167227)

Gene Information

human ... NUDT12(83594)

clone

polyclonal

clone

polyclonal

clone

-

clone

3F7, monoclonal

UniProt accession no.

Q8IU60

UniProt accession no.

Q8IU60

UniProt accession no.

Q8IU60

UniProt accession no.

Q9BQG2

General description

The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors. A similar mouse protein may play a regulatory role in the acquisition of specific types of memory. It also may function as a part of a molecular clock operative in the mammalian forebrain. (provided by RefSeq)

Immunogen

NPAS2 (NP_002509, 646 a.a. ~ 738 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

Sequence
NLTTPASTSQDASQCQPSPDFSHDRQLRLLLSQPIQPMMPGSCDARQPSEVSRTGRQVKYAQSQTVFQNPDAHPANSSSAPMPVLLMGQAVLH

Physical form

Clear solution

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Verena Janes et al.
Cells, 9(3) (2020-03-07)
Genetic defects of human galactose-1-phosphate uridyltransferase (hGALT) and the partial loss of enzyme function result in an altered galactose metabolism with serious long-term developmental impairment of organs in classic galactosemia patients. In search for cellular pathomechanisms induced by the stressor

Articles

Glycosyltransferases were initially considered to be specific for a single glycosyl donor and acceptor, which led to the one enzyme-one linkage concept. Subsequent observations have refuted the theory of absolute enzymatic specificity by describing the transfer of analogs of some nucleoside mono- or diphosphate sugar donors.

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