PIPA5102589

SCCPDH Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5102589-Each-of-1 In Stock ₹ 46,502.50

PIPA5102589 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

SCCPDH

Classification

Polyclonal

Conjugate

Unconjugated

Gene

SCCPDH

Gene Alias

AW214504; C330023F11Rik; CGI 49; CGI49; CGI-49; hypothetical protein LOC507289; NET11; probable saccharopine dehydrogenase; RGD1311440; RP11-439E19.2; saccharopine dehydrogenase (putative); saccharopine dehydrogenase-like oxidoreductase; Sccpdh; SCPDH

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

109232, 305021, 51097

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide; pH 7.4

Gene Accession No.

Q6AY30, Q8NBX0, Q8R127

Gene Symbols

SCCPDH

Immunogen

A synthesized peptide derived from human SCCPDH(Accession Q8NBX0), corresponding to amino acid residues L130-F180.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Antibody detects endogenous levels of total SCCPDH
  • SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family
  • The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C
  • elegans, and maps to human chromosome 1q44
  • Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome
  • There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1
  • Stickler syndrome, Parkinson's, Gaucher disease and Usher syndrome are also associated with chromosome 1
  • A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia
  • Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.