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NSDHL Recombinant Rabbit Monoclonal Antibody [PSH02-37] (HA721814)

Price: Regular price $385.00

Volume

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Catalog# HA721814

Rabbit Monoclonal to NSDHL

Tested for

  • WB

  • IHC-P

  • IF-Cell

  • FC

Reacts with

  • Human

  • Mouse

  • Rat

Recombinant production enables lot-to-lot consistency and is animal-cruelty-free

Specifications

Product Type

Recombinant Rabbit monoclonal primary

Product Name

NSDHL Recombinant Rabbit Monoclonal Antibody [PSH02-37] (HA721814)

Immunogen

Recombinant protein within human nsdhl aa 1-300 / 373 (q15738).

Host

Rabbit

Positive Control

HeLa cell lysate, HepG2 cell lysate, A431 cell lysate, HEK-293 cell lysate, AGS cell lysate, MCF7 cell lysate, MDA-MB cell lysate, human liver tissue lysate, rat liver tissue lysate, human colon cancer tissue, human liver cancer tissue, human liver tissue, human stomach cancer tissue, mouse liver tissue, rat liver tissue, HepG2.

Conjugation

Unconjugated

Clonality

Monoclonal

Clone Number

PSH02-37

RRID

AB_3072926

APPLICATION DILUTION

  • WB

  • 1:1,000

  • IHC-P

  • 1:200-1:1,000

  • IF-Cell

  • 1:100

  • FC

  • 1:1,000

PROPERTIES

Form

Liquid

Storage Condition

Store at +4C after thawing. Aliquot store at -20C. Avoid repeated freeze / thaw cycles.

Storage Buffer

PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

Concentration

1ug/ul

Purification

Protein A affinity purified.

Molecular Weight

Predicted band size: 42 kDa

Isotype

IgG

TARGET

UNIPROT #

Q15738

PROTEIN NAME

NSDHL

SYNONYMS

decarboxylating antibody;H105E3 antibody;H105e3 protein antibody;NAD(P) dependent steroid dehydrogenase like antibody;NSDHL antibody;NSDHL_HUMAN antibody;Protein H105e3 antibody;SDR31E1 antibody;Short chain dehydrogenase/reductase family 31E member 1 antibody;Sterol 4 alpha carboxylate 3 dehydrogenase decarboxylating antibody;Sterol-4-alpha-carboxylate 3-dehydrogenase antibody;XAP104 antibody

SUBCELLULAR LOCATION

Endoplasmic reticulum membrane; Lipid droplet

FUNCTION

NSDHL is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.

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