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Bethyl Laboratories

NELFA Polyclonal Antibody

View all (12) WHSC2 antibodies

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Datasheet
Protocols
Questions & Answers

Cite NELFA Polyclonal Antibody

  • Antibody Testing Data (2)
NELFA Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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NELFA Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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NELFA Antibody (A301-910A) in IHC (P)

Detection of human NELFA by immunohistochemistry. Sample: FFPE section of human placenta. Antibody: Affinity purified rabbit anti-NELFA (Product # A301-910A) (Lot 1) used at a dilution of 1:1,000 (1 µg/mL). Detection: DAB. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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NELFA Antibody in Immunohistochemistry (Paraffin) (IHC (P))
NELFA Antibody in Western Blot (WB)
NELFA Polyclonal Antibody

Product Details

A301-910A

Applications
Tested Dilution
Publications

Western Blot (WB)

1:2,000-1:10,000
-

Immunohistochemistry (IHC)

1:500-1:2,000
-

Immunohistochemistry (Paraffin) (IHC (P))

1:500-1:2,000
-

Immunoprecipitation (IP)

2-5 µg/mg lysate
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Region between residue 478 and 528 of human negative elongation factor A.
View immunogen

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Antigen affinity chromatography

Storage buffer

tris citrate/phosphate, pH 7-8

Contains

0.09% sodium azide

Storage conditions

4°C

Shipping conditions

Ambient (domestic); Wet ice (international)

Product Specific Information

The recommended shelf life for this product is 1 year from date of receipt.

Application Note: For IHC, epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

Based on 100% sequence identity, this antibody is predicted to react with Mouse

Target Information

This gene is expressed ubiquitously with higher levels in fetal than in adult tissues. It encodes a protein sharing 93% sequence identity with the mouse protein. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome. The encoded protein is found to be capable of reacting with HLA-A2-restricted and tumor-specific cytotoxic T lymphocytes, suggesting a target for use in specific immunotherapy for a large number of cancer patients. This protein has also been shown to be a member of the NELF (negative elongation factor) protein complex that participates in the regulation of RNA polymerase II transcription elongation.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: FLJ10442; FLJ25112; Negative elongation factor A; NELF-A; Wolf-Hirschhorn syndrome candidate 2 protein

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Gene Aliases: NELF-A; NELFA; P/OKcl.15; WHSC2

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UniProt ID: (Human) Q9H3P2

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Entrez Gene ID: (Human) 7469

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Function(s)
protein binding
Process(es)
transcription from RNA polymerase II promoter transcription elongation from RNA polymerase II promoter multicellular organism development negative regulation of transcription elongation from RNA polymerase II promoter positive regulation of viral transcription
It has to be done as per old AB suggested Products section.
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Performance Guarantee

If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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